Literature DB >> 16473316

A further case of opsismodysplasia with hydrocephalus.

Feliciano J Ramos1, Juan P González, Carmen Cortabarria, Eduardo Domenech, José Pérez-González, Manuel Bueno.   

Abstract

We present a case of opsismodysplasia, a very rare skeletal dysplasia, in a term newborn female who had short length, short extremities and markedly short fingers. Radiological studies demonstrated severe platyspondyly, absence of epiphyseal ossification centers, short tubular bones, especially severe in hands and feet, with metaphyseal cupping. She also had hydrocephaly, a rare finding in opsismodysplasia. In our literature review we have found 24 cases, 17 born alive and seven terminations of pregnancy (TOPs).

Entities:  

Mesh:

Year:  2006        PMID: 16473316     DOI: 10.1016/j.ejmg.2005.04.002

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  3 in total

1.  Opsismodysplasia.

Authors:  Leslie Edward S Lewis; Y Ramesh Bhat; Prashant Naik; Kanchan Sethi; K M Girisha
Journal:  Indian J Pediatr       Date:  2010-03-19       Impact factor: 1.967

2.  Opsismodysplasia: Phosphate Wasting Osteodystrophy Responds to Bisphosphonate Therapy.

Authors:  Ansab Khwaja; Shawn E Parnell; Kathryn Ness; Viviana Bompadre; Klane K White
Journal:  Front Pediatr       Date:  2015-06-22       Impact factor: 3.418

3.  Prenatal-onset INPPL1-related skeletal dysplasia in two unrelated families: Diagnosis and prediction of lethality.

Authors:  Iman Sabri Abumansour; Radiah Mahmoud Iskandarani; Alaa Edrees; Farrukh Javed; Fadwah Taher; Ghaidaa Farouk Hakeem
Journal:  Clin Case Rep       Date:  2021-05-28
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.