Stratton Parker syndrome

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]

Stratton-Parker Syndrome
Other names	Short stature wormian bones dextrocardia

Alternative names include "Growth Hormone Deficiency with Wormian Bones, Cardiac Anomaly, and Brachycamptodactyly"^[4] and "Short stature wormian bones dextrocardia"^[1]

References

1. "Short stature wormian bones dextrocardia". Check Orphan. Retrieved 2011-09-27.
2. Stratton RF, Parker MW (February 1989). "Growth hormone deficiency, wormian bones, dextrocardia, brachycamptodactyly, and other midline defects". American Journal of Medical Genetics. 32 (2): 169–73. doi:10.1002/ajmg.1320320205. PMID 2564736.
3. Simmgen, M.; Bano, G.; Nussey, S. (2006). "Growth hormone deficiency and complex congenital abnormalities: a further case of Stratton-Parker syndrome?". Endocrine Abstracts. 12. P86. Retrieved 2011-09-27.
4. "STRATTON-PARKER SYNDROME". BioGraph. Retrieved 2011-09-27.

External links