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Titolo:
FRASER SYNDROME
Autore:
OZGUNEN T; EVRUKE C; KADAYIFCI O; DEMIR C; ARIDOGAN N; VARDAR MA;
Indirizzi:
CUKUROVA UNIV,FAC MED,DEPT OBSTET & GYNECOL BALCALT ADANA 01330 TURKEY
Titolo Testata:
International journal of gynaecology and obstetrics
fascicolo: 2, volume: 49, anno: 1995,
pagine: 187 - 189
SICI:
0020-7292(1995)49:2<187:FS>2.0.ZU;2-R
Fonte:
ISI
Lingua:
ENG
Soggetto:
BILATERAL RENAL AGENESIS; SYNDACTYLY SYNDROME; CRYPTOPHTHALMOS;
Keywords:
CONSANGUINITY; RENAL AGENESIS; FRASER SYNDROME;
Tipo documento:
Note
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
8
Recensione:
Indirizzi per estratti:
Citazione:
T. Ozgunen et al., "FRASER SYNDROME", International journal of gynaecology and obstetrics, 49(2), 1995, pp. 187-189

Abstract

In a consanguineous marriage, a woman at 32 weeks' pregnancy presented with intrauterine growth retardation and bilateral renal agenesis. Fraser syndrome (cryptophthalmus syndactyly syndrome) was diagnosed based on cryptophthalmos, atresia of meatus acusticus externus in auricula, syndactyly, hypoplastic larynx, hypoplastic left lung, agenesis of urinary system and aberrant pancreas in duodenum. The syndrome is inherited as a recessive trait and the risk of recurrence is 25%.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/10/20 alle ore 09:43:07