Literature DB >> 3146298

An association of caudal malformations arising from a defect in the "axial mesoderm" developmental field.

R J Gardner1, M M Nelson.   

Abstract

We have studied two newborn infants with a remarkable genital malformation, failure of urethral development with enormous bladder distension, atresia of the distal hindgut, vertebral abnormalities, and compression deformities. This is a pattern of anomalies similar to, and probably an extension of, the association of female pseudohermaphroditism and other anomalies (FPA) described by Lubinsky [Am J Med Genet 6:123-136, 1980]. We propose that its pathogenesis involves a defect expressed in mesoderm, especially caudal mesoderm. We offer some speculation on what might be its nature, with particular reference to the theory of cell surface molecules having a role in morphogenesis. We apply the concept of the developmental field to provide a clarifying perspective.

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Year:  1986        PMID: 3146298     DOI: 10.1002/ajmg.1320250607

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  1 in total

1.  An Unusual Case of Type A Posterior Cloaca Associated with 46XX Disorder of Sexual Differentiation with Y Duplication of Urethra.

Authors:  Rahul K Gupta; Pooja Tiwari; Sandesh V Parelkar; Beejal V Sanghvi; Kedar P Mudkhedkar; Satej S Mhaskar; Rujuta S Shah
Journal:  J Indian Assoc Pediatr Surg       Date:  2022-03-01
  1 in total

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