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Results 1 - 10 of 39 for parts Weber syndrome
  1. ... appear enlarged and bulging (buphthalmos). Individuals with Sturge-Weber syndrome can have tangles of abnormal blood vessels (hemangiomas) in various parts of the eye. When these abnormal blood vessels ...
  2. ... red vascular markings on the face and other parts of the body (shown ... disorders are also associated with Sturge-Weber syndrome.
  3. Arteriovenous Malformation (AVMs) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Arteriovenous Malformations/Start Here ... Arteriovenous Malformations ... Fistulas/Specifics ... Fistulas ... National Institute of Neurological Disorders and Stroke ... From ...
  4. ... iris) and related tissues that underlie the white part of the eye (the ... with Sturge-Weber syndrome or isolated port-wine birthmark do not have ...
  5. ... abnormal blood vessels in the brain and other parts of the body Some people respond to estrogen ...
  6. Autonomic Nervous System Disorders/Learn More ... Autonomic Nervous System Disorders ... Arrhythmia/Specifics ... Arrhythmia ... People with POTS often feel lightheaded or ...
  7. ... for Rare Disorders (NORD) ClinicalTrials.gov KLIPPEL-TRENAUNAY-WEBER SYNDROME PubMed Berry SA, Peterson C, Mize W, Bloom ...
  8. Glaucoma in Children (American Association for Pediatric Ophthalmology and Strabismus)  
    Glaucoma/Children ... Glaucoma ... American Association for Pediatric Ophthalmology and Strabismus ... GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows ...
  9. Kleefstra syndrome is a disorder that involves many parts of the body. Characteristic features of Kleefstra syndrome ... Innes M, Davies C, Lopez AG, Casalone R, Weber A, Brueton LA, Navarro AD, Bralo ... syndrome supports a major contribution of EHMT1 haploinsufficiency to ...
  10. The WNT3 gene is part of a large family of WNT genes, which play critical roles in development before birth. WNT genes provide instructions for ... other serious birth defects associated with tetra-amelia syndrome type 1. More About This Health ... C, Pascu F, Stahl U, Aulepp U, Niswander L, Weber JL, Muller U. Homozygous WNT3 mutation causes tetra- ...
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