Comprehensive treatment approaches for skeletal deformities in hypophosphatasia: a case study of ALPL gene variants
Qiongjie Jiao, Guixia Ma, Qian Ni

TL;DR
This case study shows how comprehensive treatment improved chest structure and breathing in a boy with a rare genetic disorder caused by ALPL gene variants.
Contribution
The study demonstrates the effectiveness of interdisciplinary treatment for hypophosphatasia with ALPL gene variants.
Findings
Corrective surgery improved chest wall deformities and respiratory function in the patient.
Biochemical markers normalized post-surgery, with sustained low alkaline phosphatase levels.
Genetic testing and interdisciplinary care were crucial for diagnosis and long-term quality of life.
Abstract
This study presents a case report of an 11-year-old boy with hypophosphatasia due to compound heterozygous ALPL gene genetic variants, focusing on the treatment effects of comprehensive approaches for this rare genetic disorder. The patient's diagnosis was established based on respiratory distress and cough, accompanied by anterior chest wall protrusion and flattened thorax upon physical examination. Laboratory findings showed blood and cardiac abnormalities, and genetic testing identified pathogenic ALPL variants. The treatment included corrective surgery for chest wall deformities and thoracic reshaping, which led to a gradual normalization of biochemical markers postoperatively, including creatinine, calcium, magnesium, and phosphate levels, with sustained low alkaline phosphatase levels. Following surgery, respiratory function improved, as evidenced by a follow-up chest CT scan…
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Taxonomy
TopicsAlkaline Phosphatase Research Studies · Bone health and osteoporosis research · Heterotopic Ossification and Related Conditions
