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The acrocallosal syndrome in a Turkish boy
1Division of Genetics, University of Istanbul, Turkey.
Journal of Medical Genetics
|January 1, 1990
Summary
Acrocallosal syndrome, a rare genetic disorder, was observed in a 6-month-old Turkish boy. This case highlights key features like macrocephaly and polydactyly, aiding in understanding this syndrome.
Area of Science:
- Medical Genetics
- Developmental Biology
- Clinical Case Study
Background:
- Acrocallosal syndrome is a rare genetic disorder characterized by craniofacial abnormalities, intellectual disability, and limb malformations.
- The syndrome's genetic basis and inheritance patterns are not fully understood, necessitating detailed case reports.