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Sturge Weber syndrome oral manifestations

Sturge-Weber syndrome: oral and extra-oral manifestations

Summary. Sturge-Weber syndrome is a rare, congenital, neuro-oculo-cutaneous disorder which is characterised extra-orally by unilateral port wine stains on the face, glaucoma, seizures and mental retardation, and intra-orally by ipsilateral gingival haemangioma which frequently affects the maxilla or mandible. In the present case, a 15-year-old. Sturge-Weber syndrome is a rare, congenital, neuro-oculo-cutaneous disorder which is characterised extra-orally by unilateral port wine stains on the face, glaucoma, seizures and mental retardation, and intra-orally by ipsilateral gingival haemangioma which frequently affects the maxilla or mandible Sometimes oral pyogenic granuloma have been co-related with pre existing Strurge-Weber Syndrome (SWS) and diagnosed as the oral manifestation of the same [7, 8]. Sturge-Weber Syndrome is a rare..

The present paper reports three cases of Sturge-Weber syndrome with oral manifestations and management. 2. Case Presentation. Case 1. A 23-year-old male patient came to the Department of Periodontics, Sri Sai College of Dental Surgery at Vikarabad, with a chief complaint of swelling in upper front region for 4 years which was gradually increasing in size with associated bleeding gums while eating or sometimes spontaneously Abstract Sturge Weber Syndrome is a rare non hereditary congenital sporadic disorder of elusive etiology. It has It has a vast continuum of cutaneous, neurologic, ophthalmic and oral manifestations Sturge Weber Syndrome is a rare non hereditary congenital sporadic disorder of elusive etiology. It has a vast continuum of cutaneous, neurologic, ophthalmic and oral manifestations. Routine dental procedures are associated with increased jeopardy of hemorrhage making treatment in such patients an exigent task for oral health care practitioners This disorder is characterized by facial capillary malformation & other neurological condition. The oral manifestations are gingival hemangiomatosis restricting to either side in upper and lower jaw, sometimes bilateral. We report a case of SWS with oral, ocular and neurological features

Sturge-Weber syndrome is a rare nonhereditary developmental condition with neurological and skin disorder, characterized by presence of port wine stain on the face along with ocular disorders, oral manifestations and leptomeningeal angiomas. Here we present an unusual case of Sturge-Weber syndrome with osseous hypertrophy of maxilla Sturge-Weber syndrome (SWS) is a neurocutaneous disorder characterized by vascular malformations involving the brain, skin and occasionally the eyes. Dental and oral surgery for patients with SWS can be complicated by bleeding from angiomatoses. Here we describe extraction of a semi-impacted right maxillary wisdom tooth from a 24-year-old woman. Sturge-Weber syndrome (SWS) is a neurocutaneous disorder of multisystem involvement. The central nervous system (CNS) manifestations include epilepsy (75-95%), cognitive impairment and hemiparesis . Hemipresis often follows the onset of seizures and SWS is also considered as one of the risk factors for stroke in children Key Words: Encephalotrigeminal angiomatosis, Ocular manifestations, Oral manifestations, Sturge weber syndrome, Vascular lesions Key Message / Clinical Significance: Although Sturge weber syndrome is a very rare entity, yet it has serious oral complica-tions. Morbidity can range from minor bleeding to life threatening haemorrhage, hypoxia. Conclusions: Sturge‐Weber syndrome is clinically important to the periodontist because of its associated gingival vascular features and their complicating manifestations. Periodic systemic and oral examinations are recommended to identify and prevent any complications from the cranial and oral lesions

Sturge-Weber syndrome (SWS) is a congenital, sporadically occurring, neurocutaneous syndrome that presents classically with port-wine stain, leptomeningeal angiomas, and glaucoma. The systemic implications of SWS are vast and involve not only ophthalmic manifestations but also dermatologic, neurologic, and oral manifestations some individuals with Sturge Weber Syndrome. Seizures and other neurologic complications are the result of leptomeningeal angiomas. The severity of the neurological manifestations depends on the location and amount of area involved by leptomeningeal angioma. Glaucoma is also commonly seen in Sturge Weber Syndrome and is present i Sturge-Weber syndrome is a rare neurocutaneous disorder, also known as encephalotrigeminal angiomatosis. It has varied systemic and oral manifestations, and the management of oral condition in such a case is a dental practitioner's challenge Sturge Weber syndrome (SWS) is a neurocutaneous disorder that is associated with facial capillary malformation (Port wine stain [PWS]), glaucoma, and leptomeningeal angioma in its complete form. Its incidence is estimated to be 1 per 20 000-50 000 live births.1 Some authors use the term SWS to apply to incomplete forms in which only 2 of the.

Sturge-Weber syndrome: Oral and extra-oral manifestations

Encephalotrigeminal angiomatosis (Sturge-Weber syndrome) is a rather uncommon congenital condition characterized by the combination of venous angioma of the leptomeninges over the cerebral cortex with ipsilateral angiomatous lesions of the face and sometimes, the skull, jaws and oral soft tissues What is Sturge-Weber syndrome? Sturge-Weber syndrome causes abnormal blood vessels to grow in a child's face, brain or both areas. Most children with this syndrome are born with a mark (called a capillary malformation or port wine stain) on the skin of their face Sturge-Weber syndrome (SWS) is a rare congenital developmental, disorder manifesting with a facial port-wine birthmark, and a vascular malformation of the brain. It affects the skin in the distribution of the ophthalmic branch of the trigeminal nerve, The oral manifestations are unilateral and finish abruptly in the midline. Macroglossia. Sturge-Weber syndrome is a rare congenital disorder characterized by the presence of leptomeningeal angiomas, portwine stains (sharply demarcated vascular lesions that occur unilaterally along the dermatomes supplied by first two divisions of trigeminal nerve), along with ocular disorders, mental retardation, and oral involvement

Sturge-Weber syndrome (SWS) is a rare disorder characterized by the association of a facial birthmark called a port-wine birthmark, neurological abnormalities, and eye abnormalities such as glaucoma. SWS can be thought of as a spectrum of disease in which individuals may have abnormalities affecting all three of these systems (i.e. brain, skin. Sturge-Weber Syndrome is rare, non-hereditary, congenital neurocutaneous disease. Leptomeningeal hemanjiom, generally unilateral port wine nevus distributing trigeminal nerve region, ocular abnormally (glaucoma) are some parts of this syndrome. The present paper reports oral findings of Sturge-Weber syndrome (SWS), also called encephalotrigeminal angiomatosis, is a neurocutaneous disorder with angiomas that involve the leptomeninges (leptomeningeal angiomas [LAs]) and the skin of the face, typically in the ophthalmic (V1) and maxillary (V2) distributions of the trigeminal nerve. The hallmark of SWS is a facial cutaneous veno.. Sturge-Weber syndrome is a rare, congenital, neuro-oculo-cutaneous disorder which is characterised extra-orally by unilateral port wine stains on the face, glaucoma, seizures and mental retardation, a..

Gingival overgrowth associated with port-wine stains: A

Oral and extraoral manifestationse of sturge-Weber syndrome: A rare finding Amitandra K Tripathi 1, Mohammad Arif Khan 1, Krishna Deo 2, Ranjan Mani Tripathi 3 1 Department of Periodontology, Career Postgraduate Institute of Dental Sciences and Hospital, Lucknow, Uttar Pradesh, India 2 Department of Prosthodontic, Career Postgraduate Institute of Dental Sciences and Hospital, Lucknow, Uttar. Sturge-Weber syndrome - A case report. This disorder is characterized by facial capillary malformation & other neurological condition. The oral manifestations are gingival hemangiomatosis restricting to either side in upper and lower jaw, sometimes bilateral. We report a case of SWS with oral, ocular and neurological features Sturge weber syndrome is a sporadic congenital neuro cutaneous disorders. It is one of the phakomatoses and is often The oral manifestations include ipsilateral port-wine stains of oral mucosa along with the hypervascular changes. Angiomatous lesions of gingiva which can vary from slight vascular hyperplasia to.

Background: Sturge-Weber syndrome is a rare neurocutaneous condition, also known as angiomatosis of the encephalotrigeminals.It has varied systemic and oral manifestations, and the challenge for a dental practitioner is to manage oral condition in such a case Sturge-Weber syndrome has been included in the group of phakomatoses that is characterized by hamartomas involving the brain, skin, and eyes. The characteristic facial port-wine stain, involving the first branch of the trigeminal nerve and the embryonic vasculature distribution in this area, leads to several ocular complications of the anterior segment and can involve the eyelids and conjunctiva Sturge-Weber syndrome is a rare nonhereditary developmental condition with neurological and skin disorder, characterized by presence of port wine stain on the face along with ocular disorders, oral manifestations and leptomeningeal angiomas. Here we present an unusual case of Sturge-Weber syndrome with osseous hypertrophy of maxilla. 1. The Sturge- Weber syndrome More Details (SWS), also called encephalotrigeminal angiomatosis, is a neurocutaneous disorder with angiomas involving the leptomeninges [leptomeningeal angiomas (LAs)] and skin of the face, typically in the ophthalmic and maxillary distributions of the trigeminal nerve.SWS is manifested at birth by seizures accompanied by a large port-wine stain (PWS) birthmark on. A 15 Year old female patient with Sturge Weber Syndrome is presented. This neurocutaneous syndrome consists of angiomatosis of the skin and mucosa as well as the leptomeninges. This case report describes the classic presentation of the syndrome, emphasizing the oral manifestations. The radiographic and CT scan show the typical tram line intracranial calcifications

the Sturge-Weber syndrome diagnosis. However, despite the oral manifestations, as the patient complained about no symptoms, she was oriented regarding the syndrome and referred to a neurology service in order to investigate possible alterations. Case 2. A 19-year-old white female patient was referre Babies with Sturge-Weber syndrome (SWS) are born with a facial birthmark known as a port-wine stain. The color can range from dark red to light pink and it is usually found on one side of the face. In addition, people with SWS have abnormal growth of blood vessels within the tissue that covers the brain and spinal cord (leptomeningeal angioma). These angiomas can lead to decreased blood flow. Oral-facial manifestations of Klippel-Trenaunay-Weber syndrome Report of two cases James J. Sciubba, D.M.D., Ph.D.* and Ashley M. Brown, D.D.S., M.Sc.,** Stony Brook, N. T., and Bethesda, Md. STATE UNIVERSITY OF NEW YORK AT STONY BROOK AND NATIONAL CANCER INSTITUTE, NATIONAL INSTITUTES OP HEALTH Two cases of the Klippel-Trenaunay-Weber syndrome are presented

Orofacial Manifestations of Sturge-Weber Syndrom

The Sturge-Weber syndrome is a vascular dysplasia which is characterized clinically by the following classic symptoms : Major symptoms 1. A nevus flammeus of the face along the distribution of one or more branches of the trigeminal nerve. *Chief Resident, Oral Surgery, Cincinnati General Hospital, 1965-66 INTRODUCTIONThe Sturge-Weber Syndrome (SWS) or encephalotrigeminal angiomatosis, or even craniofacial angiomatosis, is specifically congenital, non-hereditary condition of rare development (1,2), although the literature presents case reports inherited in an autosomal recessive and dominant manner (3), namely of unknown etiology, marked by angiomas involving the leptomeninges and the facial.

Video: Dental Nation: Sturge-Weber Syndrome - Oral Manifestation

Sturge weber syndrome 1. + Sturge webber syndrome By Thenamudhan Ashokkumar 2. + Sturge-Weber syndrome, sometimes referred to as encephalotrigeminal angiomatosis, is a rare congenital neurological and skin disorder, non- familial disorder of unknown incidence and cause. It is characterized by a congenital facial birthmark and neurological abnormalities. Other symptoms associated with Sturge. The great frequency of oral manifestations of Sturge-Weber syndrome patients demands the dentist's knowledge of this syndrome signs and symptoms as well as the knowledge of the best treatment to be performed due to the increased risk of hemorrhage. It is important to note th Sturge-Weber Syndrome Sturge-Weber syndrome (SWS) is a segmental vascular neurocutaneous disorder with a constellation of symptoms and signs characterized by capillary malformation in the face (port-wine birthmark) and brain (leptomeninges), as well as abnormal blood vessels of the eye leading to glaucoma. Patients present with seizures, hemiparesis, stroke-like episodes, headaches, and. The Sturge-Weber Syndrome: its periodontal significance. el-Mostehy MR, Stallard RE. PMID: 5253994 [Indexed for MEDLINE] Publication Types: Case Reports; MeSH terms. Adolescent; Angiomatosis* Female; Humans; Mouth Neoplasms* Oral Manifestations* Periodontal Diseases Sturge-Weber syndrome has neurologic manifestations (cerebral anomalies), and cutaneous, ocular, and oral anomalies, which may or may not be associated; nevertheless, the most evident clinical manifestation is nevus flammeus in the face or port-wine stain, which normally follows the trajectory of the V1 and V2 branches of the trigeminal nerve.

Sturge-Weber syndrome: oral and extra-oral manifestations

Periodontal Management of Sturge-Weber Syndrom

Sturge-Weber Syndrome (SWS), also known as encephalotrigeminal angiomatosis, is a congenital neuro-oculocutaneous syndrome that presents at birth.[1] SWS was first reported by Dr. Schirmer in 1860 with later descriptions by Dr. Sturge in 1897 and Dr. Weber in 1922.[2] It is characterized as a part of the neuroectodermal dysplasias, also known as phakomatoses The aim of this case review was to touch upon the various clinical presentations and diagnostic features of Sturge-Weber syndrome (SWS) as seen in the dental/medical practice. Sturge-Weber syndrome is a rare congenital disorder that belongs to a group of disorders collectively known as the phakomatoses. Oral manifestations are unilateral. Ocular manifestations of Sturge-Weber syndrome: pathogenesis, diagnosis, and management. Abstract: Sturge-Weber syndrome has been included in the group of phakomatoses that is characterized by hamartomas involving the brain, skin, and eyes. The characteristic facial port-wine stain, involving the first branch of the trigeminal nerve and the.

The Sturge-Weber syndrome is characterized by the presence of a leptomeningeal hemangioma variably associated with a facial nevus flammeus, seizure disorder, mental retardation, hemiparesis, homonymous hemianopsia, glaucoma, and other signs and symptoms. The relationship between the cutaneous. Yukna RA, Cassingham RJ, Carr RF: Periodontal manifestations and treatment in a case of Sturge-Weber syndrome. Oral Surg gingiva and then a CO2 laser contoured the alveolar Oral Med Oral Pathol 47:408, 1979 mucosa, allowing for good hemostasis. Estimated 7. Hylton RP: Use of CO2 laser for gingivectomy in a patient with blood loss was 1,300 mL.7.

Sturge Weber Syndrome- A Case Repor

Sturge-Weber syndrome - A case repor

What is Sturge-Weber syndrome? Sturge-Weber syndrome causes abnormal blood vessels to grow in a child's face, brain or both areas. Most children with this syndrome are born with a mark (called a capillary malformation or port wine stain) on the skin of their face. How severe Sturge-Weber syndrome is varies from child to child, but it may cause seizures, vision problems or developmental delays Sturge-Weber syndrome (SWS) is a rare, sporadic, progressive, congenital syndrome. In its complete trisymptomatic form, SWS is physically characterized by port-wine stains over the trigeminal area, leptomeningeal angiomas usually over the parieto-occipital region, and eye abnormalities. Clinical manifestation for infants with SWS depends on the affected organs, but can include seizures, mental. Sturge-Weber syndrome (SWS) is a rare, congenital disease which frequently involves the eye. It is important that ophthalmologists recognize this syndrome and are aware of its range of ocular manifestations syndrome. The present paper reports oral findings of a 18 years old female patient with Sturge-Weber Syndrome. Sturge-Weber Syndrome must be taken into account by dentists because of its various oral manifestations. Key words: Sturge Weber Syndrome; dentistry. genellikle te Sturge-weber syndrome (SWS) is a rare, congenital, non-familial neurocutaneous disorder. A case of SWS with involvement of oral cavity is reported. The oral findings, diagnostic strategy and treatment options are discussed

Sturge-Weber syndrome is a rare, congenital, neuro-oculo-cutaneous disorder which is characterised extra-orally by unilateral port wine stains on the face, glaucoma, seizures and mental retardation, and intra-orally by ipsilateral gingival haemangioma which frequently affects the maxilla or mandible. In the present case, a 15-year-old female patient presented with a port wine stain on the. The Sturge-Weber Syndrome was initially de-scribed by Schirmer in 1860 and was later specified by Sturge (1878), who associated the dermatological and ophthalmic changes to the disease's neurologi-cal manifestations. In 1992 Weber complemented it through the documentation of these patients' cere-bral radiologic alterations (2) Introduction: Sturge-Weber syndrome is a rather uncommon congenital condition that occurs sporadically, characterized by the combination of ipsilateral angiomatous lesions of the face, oral soft tissues, and jaws with venous angioma of the leptomeninges over the cerebral cortex.However, the main clinical features of this syndrome are facial vascular cutaneous naevus, usually unilateral, which. The Sturge-Weber syndrome is characterized by the presence of a leptomeningeal hemangioma variably associated with a facial nevus flammeus, seizure disorder, mental retardation, hemiparesis, homonymous hemianopsia, glaucoma, and other signs and symptoms

Sturge-Weber Syndrome with Osteohypertrophy of Maxill

  1. Sturge-Weber syndrome INTRODUCTION Sturge-Weber syndrome (SWS) is a rare, congenital neuro-oculocutaneous disorder. Without popula-tion-based evidence, estimates of incidence range from one in 20000 to 50000 live births [1]. Syn-drome manifestations are varied and include unilat-eral port-wine birthmark (PWB), intracrania
  2. Classification 1. Syndromes causing white lesions in the gingiva- Focal palmoplantar and oral mucosa hyperkeratosis syndrome 2. Syndromes causing red lesions in the gingiva- Melkersson -Rosenthal syndrome, Sturge- Webber syndrome, Klippel-Trenaunay- Weber syndrome, Sjogren's syndrome, Osler- Rendu-Weber syndrome. 8
  3. Sturge-Weber syndrome: oral and extra-oral manifestations View 0 peer reviews of Sturge-Weber syndrome: oral and extra-oral manifestations on Publons Download Web of Science™ My Research Assistant : Bring the power of the Web of Science to your mobile device, wherever inspiration strikes
  4. Patil K, Guledgud MV, Sahni A. Sturge Weber Syndrome- A case report. International Journal of Dental Sciences and Research. 2015;3(3):45-47. Pagin O, Del Neri NB, Battisti MDPL, Capelozza ALA, da Silva Santos PS. Periodontal manifestations and ambulatorial management in a patient with Sturge Weber syndrome
  5. Royle HE, Lapp R, Ferrara ED (1966) The Sturge Weber Syndrome. Oral Surg Oral Med Oral Pathol 22: 490-497. 4. Comi AM (2015) Chapter 11-Sturge Weber Syndorme. In: Neurocutaneous Syndromes. 5. Arkush L, Prabhakar P, Scott RC, Aylett SE (2020) Headache in children with Sturge-Weber syndrome-prevalence, associations and impact. Eur
  6. al nerve, leptomeningeal angiomatosis and glaucoma [1, 2].Cerebral vascular malformations result in the neurological manifestations of SWS, including seizures, stroke-like episodes and intellectual.

The ocular manifestations of the Sturge-Weber syndrome. J Pediatr Ophthalmol Strabismus. 1992 Nov-Dec. 29(6):349-56. . Miller RS, Ball KL, Comi AM, Germain-Lee EL. Growth hormone deficiency in. Sturge-Weber syndrome (SWS) was first described by Oral cavity was normal. Ophthalmological evaluation was normal. Other systemic examination was normal. There was a history of seizure disorder following neurological manifestations[18,19] when seizures are not controlled by medical treatment may also be of benefit Sturge-Weber syndrome is a rare nonhereditary developmental condition that is characterized by a hamartomatous vascular proliferation involving the tissue of brain and face. Oral manifestations include unilateral blood vessel expansion of the oral mucosa, vascular hyperplasia o

Tooth extraction with Sturge-Weber syndrome - ScienceDirec

  1. Sturge-Weber syndrome is characterized by an intracranial vascular anomaly, leptomeningeal angiomatosis, most often involving the occipital and posterior parietal lobes. The most common symptoms and signs are facial cutaneous vascular malformations (port-wine stains), seizures, and glaucoma. Stasis results in ischemia underlying the leptomeningeal angiomatosis, leading to calcification and.
  2. al nerve, in its complete form, there is the association of cerebral abnormalities (leptomeningeal or pial angioma), cutaneous (facial angioma) and ocular (choroidal angioma)
  3. Sturge-Weber syndrome is a neurocutaneous syndrome that manifests with vascular malformations involving the brain, eye, and skin. We report the case of an elderly patient suffering from Sturge-Weber syndrome who presented with episodic angry slapping symptoms to a psychiatric facility
  4. ation 51 consecutive patients with a diagnosis of SWS seen at The Hospital for Sick Children.

Sturge-Weber syndrome: Continued vigilance is neede

Start studying 7. Pigmentation of the Oral Tissue. Learn vocabulary, terms, and more with flashcards, games, and other study tools Oral cavity involvement may occur, and the extent of the vascular abnormality may vary considerably. The present authors report the case of a 6-year-old girl with Sturge-Weber syndrome, focusing on the clinical and radiographic features

Sturge - Weber syndrome: A case report. Contemporary Clinical Dentistry, 2010. Namratac Gill. Nandini Bhaskar. Namratac Gill. Nandini Bhaskar. Download PDF. Download Full PDF Package. This paper. A short summary of this paper. 33 Full PDFs related to this paper. READ PAPER Sturge-Weber Syndrome (SWS) (encephelotrigeminal angiomatosis) is a congenital, non-familial disorder caused by the GNAQ gene mutation. It is characterized by a congenital facial birthmark and neurological abnormalities. Other symptoms associated with Sturge-Weber can include eye, endocrine and organ irregularities, as well as developmental. 12. Reddy SS, Kaushik A. Sturge-Weber syndrome: a case report with clinical and radiological features. J Disab Oral Health 2011; 12:39-42. 13. Khambete N, Risbud M, Kshar A. Sturge-Weber Syndrome: A Case Report. Int J Dental Clin 2011; 3:79-81. 14. Sullivan TJ, Clarke MP, Morin JD. The ocular manifestations of the Sturge-Weber syndrome. J Pediat Sturge-Weber syndrome (SWS) is a sporadic disorder and is frequent among the neurocutaneous syndromes specifically with vas-cular predominance.This syndrome consists of constellation of clinical features like facial nevus, seizures, hemiparesis, intracranial calcifications, and mental retardation

rare, sporadic neurocutaneous syndrome classically involves facial port-wine stain associated with abnormal blood vessels in brain (leptomeningeal angiomatosis) and the eye, that results in seizures, stroke-like episodes, hemiparesis, glaucoma, and visual field defects 1,2; facial birthmark plus neurological and ocular manifestations are all present in classic Sturge-Weber syndrome which. Sturge-Weber syndrome (SWS) is a neurological disorder marked by a distinctive port-wine stain on the forehead, scalp, or around the eye. This stain is a birthmark caused by an overabundance of. Photograph of a patient with Sturge-Weber syndrome; the facial hemangioma involves both upper eyelids. The patient also has glaucoma. Related. Sclerostomy obstruction. Aug 16, 2021. Tube erosion. Aug 16, 2021. Malignant glaucoma after trabeculectomy. Aug 16, 2021. Medical management, hypertrichosis.

EIN: 52-1734695. The groundbreaking identification of the gene that causes Sturge-Weber syndrome was discovered at the Kennedy Krieger Institute in 2013 by Dr. Anne Comi and her collaborators. This discovery has drastically revolutionized our medical understanding of Sturge-Weber syndrome and and laid the groundwork for clinical trials Sturge Weber syndrome (WSS), also known as trigeminal brain angiomatosis, is the most common neurocutaneous disorder. It is congenital, sporadic and does not present hereditary character or predisposition to malignant. It affects both sexes equally, having an incidence of 1 in every 50,000 live births Sturge-Weber syndrome (SWS) is a sporadic disorder and is frequent among the neurocutaneous syndromes specifically with vascular predominance. This syndrome consists of constellation of clinical features like facial nevus, seizures, hemiparesis, intracranial calcifications, and mental retardation A young woman, known to have Sturge-Weber syndrome, was admitted with headache and left hemiparesis. Neuroimaging showed chronic occlusion of the venous sinuses without evidence of acute thrombus formation, or a recent vascular event. A 29-year-old right-handed woman was admitted to Hull Royal Infirmary with left-sided weakness associated with.

Periodontal Management of Gingival Enlargement Associated

  1. al nerve and is associated with venous.
  2. Klippel-Trenaunay-Weber syndrome consists of port wine stains in both the extremities and the face, as well as, hypertrophy of bone and soft tissue along with the clinical manifestations of Sturge-Weber syndrome. The formation of solid visceral tumors primarily the kidney, adrenal gland, or liver helps to differentiate Klippel-Trenaunay-Weber.
  3. Sturge- Weber syndrome More Details (SWS) is one of the hamartomatoses or phakomatoses. It is a rare neuro-oculocutaneous disorder with an estimated incidence of one in 50,000 births. Clinically, the neurological manifestations include epilepsy, mental retardation, and hemiplegia; the ocular manifestations include glaucoma and vascular malformations of the conjunctiva, episclera, choroid.

Sturge-Weber Syndrome (Encephalotrigeminal Angiomatosis

Recurrent Thrombotic Deterioration in the Sturge-Weber Syndrome Hemiparesis, homonymous hemianopia and intellectual impairment are common features of the Sturge-Weber syndrome. While cerebrovascular thromboses have been noted with the syndrome, the pattern of recurrent thrombotic episodes producing an..

Gingival overgrowth associated with port-wine stains: A

  1. Sturge-Weber Syndrome: A Review - ScienceDirec
  2. Periodontal manifestations and treatment of Sturge-Weber
  3. Sturge-Weber Syndrome - Seattle Children's Hospita

Sturge-Weber syndrome

  1. Sturge Weber Syndrome - NORD (National Organization for
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Saint Joseph's Pediatric Dentistry Lit Review: Sturge