Literature DB >> 4011767

Oromandibular limb hypogenesis syndromes.

Z N Chicarilli, I M Polayes.   

Abstract

The oromandibular limb hypogenesis syndrome is a group of anomalies affecting the mandible, tongue, and maxilla with or without reductive limb anomalies. Their genetic origin is uncertain, and no drug-induced teratogen has been clearly identified. Although many similarities exist on both an embryologic and clinical level, distinction between these entities is appropriate. A new classification system with these principles in mind is presented. Two cases are presented of glossopalatine ankylosis with hypodactyly representing the thirteenth and fourteenth cited in the world literature. One patient presented with a fatal pulmonary hypoplasia not previously reported in association with this syndrome. Three of the 14 cases with reductive limb anomalies reported have had fatal outcomes.

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Year:  1985        PMID: 4011767     DOI: 10.1097/00006534-198507000-00003

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  3 in total

1.  A mouse homeo box gene, Hox-1.5, and the morphological locus, Hd, map to within 1 cM on chromosome 6.

Authors:  B A Mock; L A D'Hoostelaere; R Matthai; K Huppi
Journal:  Genetics       Date:  1987-08       Impact factor: 4.562

2.  Oromandibular Limb Hypogenesis Syndrome Type IIB: Case Report of Hypoglossia-Hypodactyly.

Authors:  Manasa Anand Meundi; Gopakumar R Nair; Prathima Sreenivasan; A C Raj
Journal:  Case Rep Dent       Date:  2013-02-04

3.  Oromandibular-limb Hypogenesis Syndrome Type II C: A Rare Case.

Authors:  Renita Lorina Castelino; Shishir Ram Shetty; Subhas Babu G; Kumuda Arvind Rao H T
Journal:  J Dent Res Dent Clin Dent Prospects       Date:  2010-12-21
  3 in total

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