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DeCS
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Descriptor Inglés:
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Weill-Marchesani Syndrome
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Descriptor Español:
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Síndrome de Weill-Marchesani
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Descriptor Portugués:
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Síndrome de Weill-Marchesani
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Sinónimos Inglés:
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Congenital Mesodermal Dysmorphodystrophy
GEMSS
Glaucoma-Lens Ectopia-Microspherophakia-Stiffness-Shortness Syndrome
Marchesani Syndrome
Marchesani-Weill Syndrome
Spherophakia-Brachymorphia Syndrome
Weill-Marchesani Syndrome, Autosomal Dominant
Congenital Mesodermal Dysmorphodystrophies
Dysmorphodystrophies, Congenital Mesodermal
Dysmorphodystrophy, Congenital Mesodermal
Marchesani Weill Syndrome
Marchesani-Weill Syndromes
Mesodermal Dysmorphodystrophies, Congenital
Spherophakia Brachymorphia Syndromes
Syndrome, Spherophakia Brachymorphia
Syndromes, Spherophakia Brachymorphia
Weill Marchesani Syndrome, Autosomal Dominant
Weill Marchesani Syndrome, Autosomal Recessive
Mesodermal Dysmorphodystrophy, Congenital
Spherophakia Brachymorphia Syndrome
Weill Marchesani Syndrome
Weill-Marchesani Syndrome, Autosomal Recessive
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Categoría:
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C05.116.099.343.957
C11.270.921
C16.131.077.941
C16.320.290.842
C17.300.899
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Definición Inglés:
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Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen. |
Relacionados Inglés:
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Marfan Syndrome
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Nota Histórica Inglés:
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2010
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Calificadores Permitidos Inglés:
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Número del Registro:
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53490
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Identificador Único:
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D056846
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Ocurrencia en la BVS:
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Similar:
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DeCS CID-10 LILACS
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