Musculoskeletal manifestations of neonatal nonketotic hyperglycinemia
- Norman RamirezAffiliated withPediatric Orthopedic Department, Mayagüez Medical Center Email author
- , John M. FlynnAffiliated withPediatric Orthopaedic Department, Hospital de la Concepción
- , Francisco CasalducAffiliated withSchool of Medicine, Universidad Central del Caribe
- , Stephanie RodriguezAffiliated withInterAmerican University
- , Alberto S. CornierAffiliated withGenetic Department, Molecular Laboratory, Hospital de la Concepcion
- , Simón CarloAffiliated withGenetic Department, Molecular Laboratory, Hospital de la Concepcion
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Neonatal nonketotic hyperglycinemia is an autosomal recessive inborn disorder of glycine metabolism in which large quantities of glycine accumulate in all body tissues. It is characterized by a progressive lethargy, hypotonia, myoclonic jerks, and early death secondary to respiratory problems. As a result of early diagnosis and treatment protocols, more patients survive the critical neonatal period with profound mental retardation, delayed developmental milestones, seizures, and spasticity. There are no reports about the orthopaedic manifestations of neonatal nonketotic hyperglycinemia. The purpose of this study is to evaluate the musculoskeletal findings of neonatal nonketotic hyperglycinemia.
This is a retrospective IRB-approved study of all patients in our Orthopaedic and Genetics Clinics with the diagnosis of neonatal nonketotic hyperglycinemia during a 10-year period. Demographic, clinical, and imaging data were analyzed.
Twelve patients with neonatal nonketotic hyperglycinemia were evaluated, with a mean age of 7 years and 2 months (range: 5 months to 21 years). Seven were male and five were female. Eleven patients (92 %) have evidence of progressive early-onset neuromuscular scoliosis with a mean Cobb angle of 55° (range: 30–95°). Five children (42 %) presented evidence of progressive hip dislocation secondary to spasticity. All the patients have severe multiple joint contractures.
Neonatal nonketotic hyperglycinemia is a rare metabolic disorder presented in the past as a lethal condition. Recent advances in early diagnosis and neonatal care improve overall outcome. As pediatric orthopaedic surgeons, we need to establish treatment based on update information of the disease and probability to improve quality of life.
KeywordsMetabolic disorder Scoliosis Joint contractures Hip dislocation
- Musculoskeletal manifestations of neonatal nonketotic hyperglycinemia
Journal of Children's Orthopaedics
Volume 6, Issue 3 , pp 199-203
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- Metabolic disorder
- Joint contractures
- Hip dislocation
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- Author Affiliations
- 1. Pediatric Orthopedic Department, Mayagüez Medical Center, Box 6847, Mayagüez, PR, 00681, USA
- 2. Pediatric Orthopaedic Department, Hospital de la Concepción, San Germán, PR, USA
- 3. School of Medicine, Universidad Central del Caribe, Bayamón, PR, USA
- 4. InterAmerican University, San Germán, PR, USA
- 5. Genetic Department, Molecular Laboratory, Hospital de la Concepcion, San Germán, PR, USA