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1.
Tunisie Medicale [La]. 2012; 90 (12): 902-903
em Francês | IMEMR | ID: emr-155950
2.
Maghreb Medical. 2005; 25 (375): 194-195
em Francês | IMEMR | ID: emr-171445

RESUMO

Amelia is a rare syndrome characterized by complete absence of one or all four limbs. We reported two cases of amelia observed in service A of the CMNT during 2002. The purpose of this article is to discuss the different etiologies of this malformation and to underline the contribution of the ultrasound done early [12 weeks of gestation]. Amelia is the result of toxic, mechanic or genetic causes. The antenatal diagnosis by ultrasonography is very useful

8.
Tunisie Medicale [La]. 2000; 78 (12): 727-730
em Francês | IMEMR | ID: emr-55968

RESUMO

Letal spina bifida continue to be frequent in Tunisia; we report 88 cases of letal spina bifida 1,05 per thousand births. This pathology was more frequent with women. The up letal spina bifida situated is predominant with female and the dow spina bifida situated is frequent with male. We have noted an association with anencephalia [46 cases] and hydrocephaly [21 cases]. Prevention is based on obstetric health care and hygieno dietetic advices to avoid alimentary deficit


Assuntos
Humanos , Masculino , Feminino , Feto/patologia , Ultrassonografia Pré-Natal , Ácido Fólico , Anencefalia , Hidrocefalia , Estudos Retrospectivos
9.
Tunisie Medicale [La]. 2000; 78 (8-9): 538-541
em Francês | IMEMR | ID: emr-56011

RESUMO

we report one case of congenital cystic adenomatoid malformation of the lung [C.A.A.M.] diagnosed at 24 weeks of gestation with concomitant fetal hydraps. The diagnosis of [C.A.A.M.] type I was confirmed histologically


Assuntos
Humanos , Feminino , Ultrassonografia Pré-Natal , Pulmão , Hidropisia Fetal
10.
Tunisie Medicale [La]. 1996; 74 (8-9): 358-60
em Francês | IMEMR | ID: emr-43611

RESUMO

The Mckusick Kaufman syndrome is a rare autosomal recessive disorder characterised by a triad of hydrometrocolpos, post axial polydacryly and congenital heart disease. Multiple other anomalies may be associated. A great phenotypic variability ocurs in this syndrome make it very difficult to identify and classify it correctly. A new observation of this syndrome is presented in a female full term new-born of first cousin parents. The prenatal diagnosis of the hydrocolpos is done at the 12 weeks of gestation. Both hydrocolpos and post axial polydactyly allowed to carry the diagnostic of the Mckusick syndrome in this observation without congenital heart disease


Assuntos
Polidactilia , Cardiopatias Congênitas , Diagnóstico Pré-Natal
11.
Tunisie Medicale [La]. 1988; 66 (2): 93-97
em Francês | IMEMR | ID: emr-11873

RESUMO

In order of a better normal human digestive mucins codification, we have undertook a histochemical approach of these mucins on biopsical samples of normal digestive mucus and on the principal salivary glands. A comparative study was realized on the f'tal tissues and colic and gastric adenocarcinomatous tumors, Identification of different reactions of the mucins nature were utilized. In the Salivary glands, the secreted mucins by mucous portion are of acid type richly sulfated. On the level of the digestive tube, the stomach epithelium, the cardial and antropyloric glands and either the duodenum Brunner Glands elaborate the neutral mucins [fucomucins]


Assuntos
Histocitoquímica
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