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Results: 4

1.

Weber-Gubler syndrome

MedGen UID:
96812
Concept ID:
C0455717
Disease or Syndrome
2.

Sturge-Weber syndrome

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 laminar cortical necrosis. The clinical course is highly variable and some children experience intractable seizures, mental retardation, and recurrent stroke-like episodes (review by Thomas-Sohl et al., 2004). [from OMIM]

MedGen UID:
21361
Concept ID:
C0038505
Congenital Abnormality
3.

Syndrome

A set of symptoms or conditions that occur together and suggest the presence of a certain disease or an increased chance of developing the disease. [from NCI]

MedGen UID:
11688
Concept ID:
C0039082
Disease or Syndrome
4.

Error occurred: cannot get document summary

ID:
449908

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