Two Cases of Seckel Syndrome / 대한소아내분비학회지
Journal of Korean Society of Pediatric Endocrinology
;
: 228-230, 1998.
Artigo
em Coreano
| WPRIM
| ID: wpr-42959
ABSTRACT
Seckel syndrome is a rare, autosomal recessive disorder of severe growth retardation and distinct craniofacial, orodental, and skeletal anomalies. We report hereby the first two Korean cases of typical Seckel syndrome who had characteristic symptoms of intrauterine growth retardation, small head, large eyes, sharp facial features (beaked nose, dysplastic ears and narrow face) with underdeveloped chin, dwarfism, severe mental retardation, and other malformation. We report two cases of Seckel syndrome with a brief review of related literatures.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Nariz
/
Queixo
/
Nanismo
/
Orelha
/
Retardo do Crescimento Fetal
/
Cabeça
/
Deficiência Intelectual
Idioma:
Coreano
Revista:
Journal of Korean Society of Pediatric Endocrinology
Ano de publicação:
1998
Tipo de documento:
Artigo
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