A New Born with Lamellar ichthyosis(Collodion Baby).
نویسندگان
چکیده
Ichthyosisis an infrequent clinical entity worldwide with an incidence of 1:600,000 births. It can be one of the two types: collodion baby and Harlequin fetus or malignant keratoma (most severe form). The clinical manifestations in either form are thick and hard skin with deep splits. Affected babies are born in a collodion membrane, a shiny waxy outer layer to the skin that is shed 10 - 14 days after birth, revealing the main symptom of the disease. The reported case is of a neonate, born to primigravida mother at seven and a half month's gestation with a birth weight of 2160 grams and Apgar score of 6/10 and 8/10 at 1 and 5 minutes respectively. Conclusively, early diagnosis of this condition can help cope and prevent serious morbidity or even mortality at time. These newborns should be monitored carefully in intensive care units by a multi-disciplinary team.
منابع مشابه
Collodion Baby with TGM1 gene mutation
Collodion baby (CB) is normally diagnosed at the time of birth and refers to a newborn infant that is delivered with a lambskin-like membrane encompassing the total body surface. CB is not a specific disease entity, but is a common phenotype in conditions like harlequin ichthyosis, lamellar ichthyosis, nonbullous congenital ichthyosiform erythroderma, and trichothiodystrophy. We report a CB tha...
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INTRODUCTION Lamellar ichthyosis (collodion baby) is a cornification disorder classified under the category of autosomal recessive congenital ichthyosis and characterized by hyperkeratosis. Early-stage retinoid treatment has been shown to improve survival in these patients. In this article, a lamellar ichthyosis case is presented of an infant who had the symptoms at birth and was treated succes...
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ورودعنوان ژورنال:
- Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
دوره 25 8 شماره
صفحات -
تاریخ انتشار 2015