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Porencephaly in a fetus and HANAC in her father: variable expression of COL4A1 mutation.
Takenouchi, Toshiki; Ohyagi, Masaki; Torii, Chiharu; Kosaki, Rika; Takahashi, Takao; Kosaki, Kenjiro.
Afiliación
  • Takenouchi T; Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
Am J Med Genet A ; 167A(1): 156-8, 2015 Jan.
Article en En | MEDLINE | ID: mdl-25425218
COL4A1-associated disorders encompass a wide range of hereditary vasculopathy, including porencephaly and HANAC (adult-onset hemorrhagic stroke with cerebral aneurysm and retinal arterial tortuosity, renal cysts, and thenar muscle cramp). It remains elusive whether or not porencephaly and HANAC are molecularly distinctive disorders due to different classes of mutations. We report on a girl with porencephaly and an episode of microangiopathic hemolysis in infancy and her father with HANAC, both of whom had a heterozygous missense mutation of COL4A1 (c.3715G>A, p.G1239R). The current observation implies phenotypic diversities of COL4A1 mutations.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Raynaud / Colágeno Tipo IV / Padre / Feto / Porencefalia / Calambre Muscular / Mutación Límite: Adult / Female / Humans / Infant / Male / Newborn / Pregnancy Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Raynaud / Colágeno Tipo IV / Padre / Feto / Porencefalia / Calambre Muscular / Mutación Límite: Adult / Female / Humans / Infant / Male / Newborn / Pregnancy Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Japón