Caricamento...
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....
Salvato in:
| Pubblicato in: | Pan Afr Med J |
|---|---|
| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
The African Field Epidemiology Network
2016
|
| Soggetti: | |
| Accesso online: | 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 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|