Omphalocele in half-siblings
Autor: | A. B. Scott-Emuakpor, Saroj Kapur, James V. Higgins, Eugene A. Dolanski |
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Rok vydání: | 2008 |
Předmět: |
Male
medicine.medical_specialty Pediatrics Fetus Omphalocele business.industry media_common.quotation_subject Infant Prenatal diagnosis medicine.disease Pedigree Endocrinology Child Preschool Internal medicine Genetics medicine Humans Female Girl business Hernia Umbilical Genetics (clinical) media_common |
Zdroj: | Clinical Genetics. 18:88-90 |
ISSN: | 1399-0004 0009-9163 |
DOI: | 10.1111/j.1399-0004.1980.tb01370.x |
Popis: | A family is described in which half-siblings, a boy and a girl born to unrelated mothers and a phenotypically normal father, were affected with omphalocele. The suggested mode of transmission remains unclear. Prenatal diagnosis to detect an affected fetus should be offered to relatives of omphalocele-affected individuals. |
Databáze: | OpenAIRE |
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