Literature DB >> 11152148

Situs inversus totalis and congenital hypoglossia.

D J Amor1, J E Craig.   

Abstract

Hypoglossia is a rare congenital malformation, occurring either as an isolated malformation or in association with other deformities, particularly limb defects. We describe a female infant with congenital hypoglossia, micrognathia and situs inversus. The main complications were airway compromise and feeding difficulties requiring tracheostomy and gastrostomy. Situs inversus and hypoglossia have been reported together on six previous occasions, with all cases being sporadic. Situs inversus-hypoglossia falls into a spectrum of aetiologically non-specific developmental field defects that includes the Aglossia-adactylia spectrum and the Agnathia-holoprosencephaly spectrum. Situs inversus-hypoglossia may represent a mild form of Agnathia-holoprosencephaly.

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Year:  2001        PMID: 11152148     DOI: 10.1097/00019605-200101000-00010

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  2 in total

Review 1.  Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology.

Authors:  Thomas M Maynard; Irene E Zohn; Sally A Moody; Anthony-S LaMantia
Journal:  Annu Rev Neurosci       Date:  2020-02-26       Impact factor: 12.449

2.  Isolated aglossia in a six year old child presenting with impaired speech: a case report.

Authors:  Altaf Rasool; Mohammad Inam Zaroo; Adil Hafeez Wani; Mohammad Ashraf Darzi; Shiekh Adil Bashir; Akram Hussain Bijli; Shafaq Rashid
Journal:  Cases J       Date:  2009-09-17
  2 in total

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