Meckel Gruber syndrome – a case report
Abstract Background Meckel Gruber Syndrome (MKS) is a rare autosomal recessive malformation syndrome characterized by multiple congenital anomalies ultimately leading to the death of fetus in utero or shortly after birth. It is characterized by classical triad of occipital encephalocele, infantile p...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2020-04-01
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| Series: | Surgical and Experimental Pathology |
| Subjects: | |
| Online Access: | http://link.springer.com/article/10.1186/s42047-020-00062-3 |