Cerebral palsy laboratory findings

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Iqra Qamar M.D.[2]

Overview

There are no diagnostic laboratory findings associated with cerebral palsy. The American Academy of Neurology (AAN) recommends lab studies if there is no specific structural abnormality present-, the presence of atypical features in history or physical examination and cerebral palsy associated with brain malformation. Following labs may help to rule out other diseases and may include thyroid function tests, lactate and pyruvate levels, organic and amino acids, ammonia levels and chromosomal analysis.

Laboratory Findings

References

  1. Ashwal S, Russman BS, Blasco PA, Miller G, Sandler A, Shevell M, Stevenson R (2004). "Practice parameter: diagnostic assessment of the child with cerebral palsy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society". Neurology. 62 (6): 851–63. PMID 15037681.
  2. Pons R, Collins A, Rotstein M, Engelstad K, De Vivo DC (2010). "The spectrum of movement disorders in Glut-1 deficiency". Mov. Disord. 25 (3): 275–81. doi:10.1002/mds.22808. PMID 20063428.
  3. Senbil N, Yüksel D, Yilmaz D, Gürer YK (2007). "Prothrombotic risk factors in children with hemiplegic cerebral palsy". Pediatr Int. 49 (5): 600–2. doi:10.1111/j.1442-200X.2007.02424.x. PMID 17875083.
  4. Simchen MJ, Goldstein G, Lubetsky A, Strauss T, Schiff E, Kenet G (2009). "Factor v Leiden and antiphospholipid antibodies in either mothers or infants increase the risk for perinatal arterial ischemic ]journal=Stroke". 40 (1): 65–70. doi:10.1161/STROKEAHA.108.527283. PMID 18927445.

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