Acromegaloid facial appearance (AFA) syndrome: Report of a second family

Bruno Dallapiccola, Leopoldo Zelante, Laura Accadia, Rita Mingarelli

Research output: Contribution to journalArticle

Abstract

A family is reported in which the 'acromegaloid facial appearance' (AFA) phenotype was segregating through two generations. The five affected persons showed a striking resemblance to the patients previously reported, including progressively coarse acromegaloid-like facial appearance, narrow palpebral fissures, bulbous nose, and thickening of the lips and intraoral mucosa, resulting in exaggerated rugae and frenula. These patients also had increased birth weight and dull mentality. It is unclear if the differences between the two families mark distinct syndromes or simply extend the AFA phenotype.

Original languageEnglish
Pages (from-to)419-422
Number of pages4
JournalJournal of Medical Genetics
Volume29
Issue number6
Publication statusPublished - 1992

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Phenotype
Eyelids
Lip
Nose
Birth Weight
Mucous Membrane
Acromegaloid facial appearance syndrome

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Acromegaloid facial appearance (AFA) syndrome : Report of a second family. / Dallapiccola, Bruno; Zelante, Leopoldo; Accadia, Laura; Mingarelli, Rita.

In: Journal of Medical Genetics, Vol. 29, No. 6, 1992, p. 419-422.

Research output: Contribution to journalArticle

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