Hip Dysplasia in a Patient in Late Adolescence With Charcot-Marie-Tooth and Multiple Acyl-CoA Dehydrogenase Deficiency

Amirmohammad Heidari, Cameron Stephen, Benan Dala-Ali, Jane Webber, Oliver Pearce, Mohamed H. Ahmed


This case report explores a unique presentation of hip dysplasia in a female patient aged 21 years old diagnosed with Charcot-Marie-Tooth disease (CMT) type 1A and multiple acyl-CoA dehydrogenase deficiency (MADD). The coexistence of these neuromuscular and metabolic disorders in a patient with hip dysplasia provides an opportunity to investigate their potential interactions and impact on diagnosis, treatment, and prognosis. The patient underwent labral repair with shelf osteotomy and later a total hip replacement. This case highlights the need for further research to better understand the relationships between CMT, MADD, neuromuscular dysplasia, and hip dysplasia. A deeper understanding of these interactions may lead to improved diagnostic techniques, earlier intervention, and personalized treatment approaches for patients with co-morbid conditions, ultimately improving patient outcomes and reducing complications later in life.

J Med Cases. 2024;15(1):20-25
doi: https://doi.org/10.14740/jmc4174


Charcot-Marie-Tooth; Multiple acyl-CoA dehydrogenase deficiency; Hip prosthesis implantation; Orthopedics; Hip dysplasia

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