Glutaric aciduria type 1 presenting as bilateral subdural hematomas mimicking nonaccidental trauma. Case report and review of the literature.

Glutaric aciduria type 1 (GA1) is a rare neurometabolic disorder with characteristic neuroimaging and clinicopathological features. The authors describe a case of GA1 in a 7-month-old girl presenting with macrocephaly and bilateral subdural hematomas (SDHs) who was initially evaluated for nonaccidental trauma (NAT). Bilateral subdural drains were placed because of significant mass effect from the chronic SDHs, with subsequent neurological and neuroimaging-documented improvement. Clinical and neuroimaging findings led to further laboratory investigation to confirm the diagnosis of GA1, after which a specialized low-protein diet was initiated. After a thorough investigation, NAT was ruled out. At the follow-up examination, the patient experienced improvement in her symptoms and resolution of the bilateral subdural collections. The presence of bilateral SDHs in an infant raises the suspicion of NAT and presents a difficult diagnostic challenge because of the legal and social implications. Glutaric aciduria type 1 should be considered in the differential diagnosis of bilateral SDHs, and an evaluation should be performed. The authors review the clinical manifestations, diagnosis, medical and surgical management, and specific considerations regarding GA1, including misdiagnosis of NAT.

[1]  B. Kreft,et al.  Subdural hemorrhage as an initial sign of glutaric aciduria type 1: A diagnostic pitfall , 1996, Pediatric Radiology.

[2]  K. Lyons,et al.  Bilateral Pallidotomy for Severe Dystonia in an 18-Month-Old Child with Glutaric Aciduria , 2004, Stereotactic and Functional Neurosurgery.

[3]  Allen W Elster Glutaric aciduria type I: value of diffusion-weighted magnetic resonance imaging for diagnosing acute striatal necrosis. , 2004, Journal of computer assisted tomography.

[4]  H. Mandel,et al.  Glutaric aciduria type I , 2004, Neuroradiology.

[5]  George A. Williams,et al.  Intraretinal hemorrhages and chronic subdural effusions: glutaric aciduria type 1 can be mistaken for shaken baby syndrome. , 2003, Retina.

[6]  J. Piatt,et al.  Glutaric aciduria type 1 and nonaccidental head injury. , 2002, Pediatrics.

[7]  L. Hartley,et al.  Glutaric aciduria type 1 and nonaccidental head injury. , 2001, Pediatrics.

[8]  E. Jellum,et al.  Children with Bilateral Temporal Arachnoid Cysts may have Glutaric Aciduria Type 1 (GAT1); Operation Without Knowing that may be Harmful , 2000, Acta Neurochirurgica.

[9]  J. Zschocke,et al.  Glutaric aciduria type I: From clinical, biochemical and molecular diversity to successful therapy , 1999, Journal of Inherited Metabolic Disease.

[10]  J. Leonard,et al.  Glutaric aciduria and suspected child abuse , 1999, Archives of disease in childhood.

[11]  M. Schwartz,et al.  The human glutaryl-CoA dehydrogenase gene: report of intronic sequences and of 13 novel mutations causing glutaric aciduria type I , 1998, Human Genetics.

[12]  W Lehnert,et al.  Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. , 1996, Neuropediatrics.

[13]  Kristina J. Liu,et al.  Report of two cases , 1995 .

[14]  Z. Jamjoom,et al.  Bilateral arachnoid cysts of the sylvian region in female siblings with glutaric aciduria type I. Report of two cases. , 1995, Journal of neurosurgery.

[15]  H. Osaka,et al.  Chronic subdural hematoma, as an initial manifestation of glutaric aciduria type-1 , 1993, Brain and Development.

[16]  S. Ishii,et al.  [A pathogenesis of chronic subdural hematoma; it's relationship to subdural membrane]. , 1992, No shinkei geka. Neurological surgery.

[17]  C. Greenberg,et al.  Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds. , 1991, The Journal of pediatrics.

[18]  B. McClarty,et al.  CT‐scan Findings in an Infant with Glutaric Aciduria Type I , 1988, Developmental medicine and child neurology.

[19]  D. Trauner,et al.  Glutaric aciduria Type II. , 1980, The Journal of pediatrics.

[20]  C. Roy,et al.  [Folic acid deficiency and depression of cellular immunity]. , 1980, Archives francaises de pediatrie.

[21]  S. Markey,et al.  Glutaric aciduria; a "new" disorder of amino acid metabolism. , 1975, Biochemical medicine.