Kenny-Caffey syndrome.
Indian J Hum Genet
;
2006 May; 12(2): 96-98
Artigo
em Inglês
| IMSEAR
| ID: sea-143306
ABSTRACT
Kenny-Caffey syndrome is a rare hereditary skeletal syndrome characterized by dysmorphic features, severe growth retardation, classical radiological changes and hypocalcemia with hypoparathyroidism at an early age. We report an 8-month-old girl child with Kenny-Caffey syndrome who had most of the features of the syndrome. Any child with hypocalcemia who has typical facial features should raise a suspicion of this syndrome.
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Índice:
IMSEAR (Sudeste Asiático)
Idioma:
Inglês
Revista:
Indian J Hum Genet
Ano de publicação:
2006
Tipo de documento:
Artigo
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