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https://hdl.handle.net/11499/4431
Title: | A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies | Authors: | Ergin, Hacer Semerci, Cavidan Nur Bican, M. Düzcan, Füsun Yagci, A.B. Erdogan, K.M. Tufan, Ahmet Çevik |
Keywords: | Fibular a/hypoplasia (FA/H) Hox genes Proximal femoral focal deficiency (PFFD) Urogenital anomalies article birth weight body height bone radiography case report chromosome analysis cryptorchism disease association embryo development fibula aplasia foot radiography gestational age human hypospadias infant leg malformation male physical examination proximal femoral focal deficiency syndactyly urogenital tract malformation Abnormalities, Multiple Cryptorchidism Ectromelia Femur Fibula Genes, Homeobox Homeodomain Proteins Humans Hypospadias Infant, Newborn Karyotyping Male Mutation |
Abstract: | Malformations of the lower limbs are rare and heterogeneous anomalies. Some congenital anomalies involving face, gastrointestinal system, skeletal system, urogenital system, heart, lung and diaphragma associated with lower limb malformations have been described in the literature. Here, we report a case of left proximal femoral focal deficiency (PFFD) together with fibular aplasia associated with left undescended testis and hypospadias. The putative embryologic mechanisms of lower limb defects and their possible association with lower urogenital tract malformations are also discussed. | URI: | https://hdl.handle.net/11499/4431 | ISSN: | 0041-4301 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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