Literature DB >> 7917123

Autosomal dominant congenital macroglossia: further delineation of the syndrome.

M C Reynoso1, A Hernández, L A Lizcano-Gil, A Sarralde, M C Abreu, Z Nazará, R Fragoso.   

Abstract

We describe seven patients from two Mexican families with congenital macroglossia. Comparative analysis of these cases and the patients previously described in literature, allows to confirm the notion that this isolated primary macroglossia is a distinct dominant condition.

Entities:  

Mesh：

Year:  1994        PMID： 7917123

Source DB:  PubMed          Journal:  Genet Couns        ISSN： 1015-8146


  3 in total

1.  Family aggregation of upper airway soft tissue structures in normal subjects and patients with sleep apnea.

Authors:  Richard J Schwab; Michael Pasirstein; Laura Kaplan; Robert Pierson; Adonna Mackley; Robert Hachadoorian; Raanan Arens; Greg Maislin; Allan I Pack
Journal:  Am J Respir Crit Care Med       Date:  2005-10-06       Impact factor: 21.405

2.  Germline PRKACA amplification leads to Cushing syndrome caused by 3 adrenocortical pathologic phenotypes.

Authors:  J Aidan Carney; Charalampos Lyssikatos; Maya B Lodish; Constantine A Stratakis
Journal:  Hum Pathol       Date:  2014-10-02       Impact factor: 3.466

3.  Surgical treatment of congenital true macroglossia.

Authors:  Sabrina Araújo Pinho Costa; Mário César Pereira Brinhole; Rogério Almeida da Silva; Daniel Hacomar Dos Santos; Mayko Naruhito Tanabe
Journal:  Case Rep Dent       Date:  2013-12-05
  3 in total

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