Stratton Parker syndrome
Medical condition / From Wikipedia, the free encyclopedia
Stratton parker syndrome is a rare disorder characterized by short stature, wormian bones (extra cranial bones), and dextrocardia (displaced heart).[1] Other symptoms include dermatoglyphics, tooth deformities or missing teeth, abnormal kidney development, shortened limbs, intellectual disability, undescended testes or cryptorchidism, and anal atresia.[1] The condition was first described by Stratton and Parker in 1989,[2] and there have been only four reported cases worldwide.[3]
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Stratton-Parker Syndrome | |
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Other names | Short stature wormian bones dextrocardia |
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Alternative names include "Growth Hormone Deficiency with Wormian Bones, Cardiac Anomaly, and Brachycamptodactyly"[4] and "Short stature wormian bones dextrocardia"[1]