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Syndrome de Meckel Gruber: à propos d’un cas rare
Meckel Gruber syndrome is a rare autosomal recessive polymalformation syndrome characterized by occipital encephalocele, polydactyly and cystic renal dysplasia. Ultrasound is, at present, the best tool for prenatal screening of this lethal polymalformation and diagnosys is confirmed by karyotyping....
Guardat en:
| Publicat a: | Pan Afr Med J |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The African Field Epidemiology Network
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5268799/ https://ncbi.nlm.nih.gov/pubmed/28154732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2016.25.43.9696 |
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