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Congenital disorder of glycosylation type Ia (CDG-Ia): phenotypic spectrum of the Mental retardation, ataxia, muscular atrophy, and febrile seizures were consistent The diagnosis of CDG-Ia had been made by isoelectric focusing of serum .. (1996) Carbohydrate-deficient glycoprotein syndromes. in Handbook of
20 Aug 2014 Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) Personality disorders are clinical syndromes that tend to have
Learn about DSM–5, the standard classification of mental disorders used by mental health professionals in the U.S..
1 Dec 2001 Tf IEF is currently the most widely used method for CDG diagnosis, although automated deficiency—all of the disorders show various degrees of mental and psychomotor Other adults with mild forms of the disease can even run and draw. .. and of course single patients provide inadequate statistics.
o The Motor Disorder is a secondary diagnosis; and According to the DSM, Motor Disorders include (Diagnostic and Statistical Manual of Mental. Disorders
7 Nov 2017 PMM2-congenital disorder of glycosylation (PMM2-CDG, also known as congenital disorder of glycosylation type Ia) is an inherited condition
Diagnostic and Statistical Manual of Mental Disorders , Fifth Edition. Edited by American Psychiatric Association. Expand All|Close All

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March 2018