Literature DB >> 24800790

Campomelic dysplasia.

Vineet Jain1, Biswaroop Sen.   

Abstract

Campomelic dysplasia is a rare hereditary congenital osteochondral dysplasia characterized by abnormal bowing of the lower limbs, sex reversal in males, and other skeletal and extraskeletal abnormalities. It is usually fatal in the neonatal period because of respiratory insufficiency. The diagnosis is usually difficult because of its rare presentation and the prognosis is poor. We present such a case in a 1-month-old child with typical skeletal abnormalities, whose presentation was unusual because of later presentation of respiratory distress and lack of genitourinary abnormalities.

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Year:  2014        PMID: 24800790     DOI: 10.1097/BPB.0000000000000058

Source DB:  PubMed          Journal:  J Pediatr Orthop B        ISSN: 1060-152X            Impact factor:   1.041


  2 in total

1.  Prenatal diagnosis of fetal skeletal dysplasia using 3-dimensional computed tomography: a prospective study.

Authors:  Miyoko Waratani; Fumitake Ito; Yukiko Tanaka; Aki Mabuchi; Taisuke Mori; Jo Kitawaki
Journal:  BMC Musculoskelet Disord       Date:  2020-10-08       Impact factor: 2.362

2.  Case report: Cystic hygroma accompanied with campomelic dysplasia in the first trimester caused by haploinsufficiency with SOX9 deletion.

Authors:  Xijing Liu; Jianmin Wang; Mei Yang; Tian Tian; Ting Hu
Journal:  Front Genet       Date:  2022-08-29       Impact factor: 4.772

  2 in total

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