Adams-Oliver Syndrome: Piecing Together the Puzzle of a Rare Condition
Adams–Oliver Syndrome (AOS) is a rare congenital disorder characterized by aplasia cutis congenita and terminal transverse limb defects with an incidence of 0.44 per 100,000 live births, with genetic inheritance being autosomal dominant, recessive or sporadic. This report describes a 2-year-old girl...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wolters Kluwer Medknow Publications
2025-05-01
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| Series: | Medical Journal of Dr. D.Y. Patil Vidyapeeth |
| Subjects: | |
| Online Access: | https://journals.lww.com/10.4103/mjdrdypu.mjdrdypu_1003_24 |
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