A Case Report of Hypophosphatemic Rickets with Thoracic Myelopathy

Zenodo (CERN European Organization for Nuclear Research) 2026 Open access

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Authors: Kamal Abdulazeez Mohammadamin, Amanj Jamal Khidhir Pastaksor
DOI: 10.5281/zenodo.18396991
Cited by: 0

Abstract

Abstract Hypophosphatemic ricket is x linked dominant disease due to mutation in PHEX gene, characterized by renal phosphate wasting (i.e. inability to reabsorb phosphate). Knowledge of phosphate metabolism is critical to determine the underlying causes of hypophosphatemia and to facilitate appropriate treatment. Keywords: hypophosphatemic ricket, PHEX gene, Myelopathy.

Fields of Study & Subjects

Parathyroid Disorders and Treatments Alkaline Phosphatase Research Studies Dermatological and Skeletal Disorders

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
28 January 2026