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Meckel syndrome: genetics, perinatal findings, and differential diagnosis.
Taiwan J Obstet Gynecol. 2007 Mar;46(1):9-14. doi: 10.1016/S1028-4559(08)60100-X.
Taiwan J Obstet Gynecol. 2007.
PMID: 17389183
Free article.
Review.
Meckel syndrome (MKS) is a lethal, autosomal recessive disorder characterized by occipital encephalocele, bilateral renal cystic dysplasia, hepatic ductal proliferation, fibrosis and cysts, and polydactyly. Genetic heterogeneity of MKS has been established by three …
Meckel syndrome (MKS) is a lethal, autosomal recessive disorder characterized by occipital encephalocele, bilateral renal cyst …
[Meckel syndrome. Update on a recurrent case].
Calmelet P, Feidt X, Viville B, Olivier D, Treisser A.
Calmelet P, et al.
J Gynecol Obstet Biol Reprod (Paris). 1997;26(4):435-41.
J Gynecol Obstet Biol Reprod (Paris). 1997.
PMID: 9265071
Review.
French.
The karyotype has to be done in order to make the differential diagnosis, especially with Trisomy 13 or 18. The rate of the Meckel's syndrome's gene is 1/400. The isolation of the specific gene will be soon helpful to define the Meckel's syndrome precisely....
The karyotype has to be done in order to make the differential diagnosis, especially with Trisomy 13 or 18. The rate of the Meckel's …
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