کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3969088 | 1256548 | 2009 | 4 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Epidermólisis ampollosa distrófica recesiva y gestación
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
زنان، زایمان و بهداشت زنان
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چکیده انگلیسی
Recessive non-Hallopeau-Siemens dystrophic epidermolysis bullosa is a rare and severe inherited skin disease characterized by increased skin fragility that can also involve the mucosa. This entity is not associated with pregnancy complications. Genetic counselling must be offered, because the risk of recurrence in parents with an affected child is 25%. However, because transmission is recessive, the risk of having affected offspring in individuals with the disease is less than 1%. Therefore prenatal diagnosis is only required if the partner has a familial history of the disease or if there is consanguinity or suspected consanguinity (for example, if both families are from the same geographical area). Vaginal delivery and breast feeding are not contraindicated, but are difficult and require individual assessment and close monitoring.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Progresos de Obstetricia y GinecologÃa - Volume 52, Issue 9, September 2009, Pages 529-532
Journal: Progresos de Obstetricia y GinecologÃa - Volume 52, Issue 9, September 2009, Pages 529-532
نویسندگان
Isabel Camaño Gutiérrez, M. Dolores Montañez Quero, Olga Villar Ruiz, Paloma Vallejo Pérez, Antonio GarcÃa Burguillo, José Manuel Hernández GarcÃa, Marcela del RÃo,