Literature DB >> 855081

Macroglossia in the Beckwith-Wiedemann syndrome.

J B Grace, W M Heroman, A D Kornblut.   

Abstract

An infant with the Beckwith-Wiedemann syndrome is described, with emphasis placed on the occurrence of macroglossia and possible maxillofacial deformities. In addition to placing the syndrome among the clinical entities which result in macroglossia, attention is also brought to concurrent metabolic disorder through hypoglycemia and possible late-occurring visceral malignancy which may produce significant patient compromise.

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Mesh:

Year:  1977        PMID: 855081

Source DB:  PubMed          Journal:  Trans Sect Otolaryngol Am Acad Ophthalmol Otolaryngol        ISSN: 0161-696X


  2 in total

1.  Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature.

Authors:  M J Pettenati; J L Haines; R R Higgins; R S Wappner; C G Palmer; D D Weaver
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

2.  The Wiedemann-Beckwith syndrome in four sibs including one with associated congenital hypothyroidism.

Authors:  R Martínez y Martínez; R Ocampo-Campos; R Pérez-Arroyo; E Corona-Rivera; J M Cantú
Journal:  Eur J Pediatr       Date:  1985-01       Impact factor: 3.183

  2 in total

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