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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 ; 70(2): 147-9, mar.-abr. 1995. ilus
Article in Portuguese | LILACS | ID: lil-175833
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 (Americas) Main subject: Syndrome / Bone Diseases, Developmental / Ichthyosiform Erythroderma, Congenital / Sezary Syndrome / Dermatitis, Exfoliative / Extremities Type of study: Diagnostic study Limits: Female / Humans / Infant, Newborn Language: Portuguese Journal: An. bras. dermatol Journal subject: Dermatology Year: 1995 Type: Article

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Index: LILACS (Americas) Main subject: Syndrome / Bone Diseases, Developmental / Ichthyosiform Erythroderma, Congenital / Sezary Syndrome / Dermatitis, Exfoliative / Extremities Type of study: Diagnostic study Limits: Female / Humans / Infant, Newborn Language: Portuguese Journal: An. bras. dermatol Journal subject: Dermatology Year: 1995 Type: Article