Polydactyly Myopia Syndrome Overview
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Learn About Polydactyly Myopia Syndrome
What is the definition of Polydactyly Myopia Syndrome?
Polydactyly myopia syndrome is characterized by postaxial polydactyly (the presence of an extra digit on the side of the hand or foot by the pinky or small toe) and progressive myopia. This condition was originally described in 9 persons in 4 generations of a family in Hungary in 1986. Family history suggests autosomal dominant inheritance.
What are the alternative names for Polydactyly Myopia Syndrome?
- Polydactyly myopia syndrome
- Czeizel Brooser syndrome
- PMS
- Postaxial Polydactyly with progressive myopia
- Postaxial polydactyly-progressive myopia syndrome
Who are the top Polydactyly Myopia Syndrome Local Doctors?
Internal Medicine
Experienced in Polydactyly Myopia Syndrome
Internal Medicine
Unmc Physicians
2510 Bellevue Medical Ctr Dr,
Bellevue, NE
Languages Spoken:
English, American Sign Language, Sign Language
Accepting New Patients
Offers Telehealth
David O'dell is an Internal Medicine provider in Bellevue, Nebraska. Dr. O'dell and is rated as an Experienced provider by MediFind in the treatment of Polydactyly Myopia Syndrome. His top areas of expertise are Orthostatic Hypotension, Low Blood Pressure, Hypertension, and Glucocorticoid-Remediable Aldosteronism. Dr. O'dell is currently accepting new patients.
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What are the latest Polydactyly Myopia Syndrome Clinical Trials?
Who are the sources who wrote this article ?
Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center
What are the Latest Advances for Polydactyly Myopia Syndrome?
Polydactyly-Myopia Syndrome: Genetic and Ophthalmologic Perspectives.
Journal: Cureus
Published: April 02, 2024
Dental Anomalies in Ciliopathies: Lessons from Patients with BBS2, BBS7, and EVC2 Mutations.
Journal: Genes
Published: October 17, 2022
Tired of the same old research?
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Bardet-Biedl syndrome-7 (BBS7) shows treatment potential and a cone-rod dystrophy phenotype that recapitulates the non-human primate model.
Journal: Ophthalmic genetics
Published: March 17, 2021