Meckel-Gruber syndrome.
Article
de En
| IMSEAR
| ID: sea-46153
Meckel- Gruber syndrome is a rare lethal, autosomal disorder. It has been linked to chromosome 17. It consists of a triad of occipital meningoencephalocoele, large polycystic kidneys and post-axial polydactyly. Death is mainly due to pulmonary hypoplasia. We report this rare case which presented with many associated defects.
Texte intégral:
1
Indice:
IMSEAR
Sujet Principal:
Rétrognathie
/
Syndrome
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Malformations multiples
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Chromosomes humains de la paire 17
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Humains
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Mâle
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Nouveau-né
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Cause de décès
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Fente palatine
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Cardiomégalie
Pays comme sujet:
Asia
langue:
En
Année:
2006
Type:
Article