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Síndrome de CHILD (hemidisplasia congênita com eritrodermia ictiosiforme e defeito de membros): relato de caso / Child's syndrome (congenital hemidysplasia with icththyosiform erythroderma and limb defects): a case report
Gonçalves, Ana Paula V; Kaminsky, Silvia K; Cestari, Silmara P; Alchorne, Mauricio Mota de Avelar; Perez, Ana Beatriz Alvarez; Brunoni, Décio.
An. bras. dermatol ; An. bras. dermatol;70(2): 147-9, mar.-abr. 1995. ilus
Article in Pt | LILACS | ID: lil-175833
Responsible library: BR11.1
RESUMO
Relato de caso de uma criança apresentando síndrome de CHILD (hemidisplasia congênita com eritrodermia ictiosiforme e defeito nos membros). Aparentemente a presença de um gene mutante no cromossomo X levaria a distúrbio no metabolismo de fibroblastos da pele, tendo como consequência displasias e anomalias cutâneas, esqueléticas e viscerais
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Index: LILACS Main subject: Syndrome / Bone Diseases, Developmental / Ichthyosiform Erythroderma, Congenital / Sezary Syndrome / Dermatitis, Exfoliative / Extremities Type of study: Diagnostic_studies Limits: Female / Humans / Newborn Language: Pt Journal: An. bras. dermatol Journal subject: DERMATOLOGIA Year: 1995 Type: Article
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Index: LILACS Main subject: Syndrome / Bone Diseases, Developmental / Ichthyosiform Erythroderma, Congenital / Sezary Syndrome / Dermatitis, Exfoliative / Extremities Type of study: Diagnostic_studies Limits: Female / Humans / Newborn Language: Pt Journal: An. bras. dermatol Journal subject: DERMATOLOGIA Year: 1995 Type: Article