Literature DB >> 14556254

A new recessive syndrome with VATER-like defects, pulmonary hypertension, abnormal ears, blue sclera, laryngeal webs, and persistent growth deficiency.

Stephen R Braddock1.   

Abstract

VATER association is a term frequently used to describe children with multiple malformations. However, occasionally these children have malformations that are not typical of VATER defects and may represent unique multiple malformation syndromes with specific prognoses and recurrence risks. Two siblings with a heretofore previously undescribed multiple malformation syndrome are presented whose features include vertebral defects, cardiac abnormalities, pulmonary hypertension, laryngeal webs, blue sclerae, and persistent growth deficiency. Autosomal recessive inheritance is suggested. These cases suggest that other individuals labeled VATER association with multiple other defects should be reviewed more closely to give accurate prognosis and recurrence risk information to families. Copyright 2003 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  2003        PMID: 14556254     DOI: 10.1002/ajmg.a.20497

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Aberrant Right Subclavian Artery-Esophageal Fistula in 20-Year-Old with VATER Association.

Authors:  Satoru Kudose; Jose Pineda; Jacqueline M Saito; Louis P Dehner
Journal:  J Pediatr Intensive Care       Date:  2016-06-29

2.  CLINICAL FEATURES AND PATTERN OF FRACTURES AT THE TIME OF DIAGNOSIS OF OSTEOGENESIS IMPERFECTA IN CHILDREN.

Authors:  Evelise Brizola; Marina Bauer Zambrano; Bruna de Souza Pinheiro; Ana Paula Vanz; Têmis Maria Félix
Journal:  Rev Paul Pediatr       Date:  2017 Apr-Jun
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.