Adams-Oliver syndrome: Case report
نویسندگان
چکیده
منابع مشابه
Adams-Oliver syndrome: a case report.
We report the case of an infant with Adams-Oliver syndrome, a rare disorder characterized by aplasia cutis congenita, defects of the limbs and extremities, and cutis marmorata telangiectatica. Other associated anomalies have been reported, such as facial dysmorphism, heart defects, and disorders of the central nervous system.
متن کاملAn autopsy case of Adams-Oliver syndrome.
We report an autopsy case of a male fetus with Adams-Oliver syndrome. His mother was a healthy, 31-year-old woman and her family and past histories were unremarkable. Therapeutic termination was done at 28(+6) weeks gestational age due to oligohydramnios detected by antenatal ultrasonography. Chromosomal study revealed normal karyotype. On autopsy, characteristic transverse terminal defect of f...
متن کاملA Case of Adams-Oliver Syndrome
Received March 19, 2009, Revised July 2, 2009, Accepted for publication July 27, 2009 Reprint request to: Deborah Lee, M.D., Department of Dermatology, Busan Paik Hospital, College of Medicine, Inje University, 633-165, Gaegeum-dong, Busanjin-gu, Busan 614-735, Korea. Tel: 82-51-8906135, Fax: 82-51-897-6391, E-mail: [email protected] Ann Dermatol Vol. 22, No. 1, 2010 DOI: 10.5021/ad.2010.22...
متن کاملA Case of Adams–Oliver Syndrome
Adams-Oliver syndrome (AOS) is a rare congenital disorder with unknown etiology commonly presented with aplasia cutis and terminal limb defects. Central nervous and cardiopulmonary systems may also be affected. It is commonly inherited as an autosomal dominant disorder but autosomal recessive and sporadic cases have also been reported. Here, we present a 10-year-old boy with extensive aplasia c...
متن کاملAdams-Oliver syndrome.
A new-born male baby with typical features of Adams-Oliver syndrome (AOS) is described. Adams-Oliver syndrome is the association of aplasia cutis congenita with terminal transverse limb reduction defects with or without cutis marmorata telangiectatica congenita. The patient presented with brachydactyly involving all the digits of his hands and shortening of both big toes along with aplasia cuti...
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ژورنال
عنوان ژورنال: Srpski arhiv za celokupno lekarstvo
سال: 2011
ISSN: 0370-8179,2406-0895
DOI: 10.2298/sarh1104221k