Search results
Results from the WOW.Com Content Network
Neonatal encephalopathy (NE), previously known as neonatal hypoxic-ischemic encephalopathy (neonatal HIE or NHIE), is defined as a encephalopathy syndrome with signs and symptoms of abnormal neurological function, in the first few days of life in an infant born after 35 weeks of gestation.
This is a shortened version of the sixth chapter of the ICD-9: Diseases of the Nervous System and Sense Organs.It covers ICD codes 320 to 389.The full chapter can be found on pages 215 to 258 of Volume 1, which contains all (sub)categories of the ICD-9.
The DC: 0-5 is intended to be used in tandem with the Diagnostic and Statistical Manual of Mental Disorders and the International Classification of Diseases . It serves to enhance the understanding, assessment, diagnosis, and treatment of mental health problems in young children by addressing the identification of disorders not adequately ...
Congenital Disorder of Glycosylation (CDG) Congenital hyperinsulinism; Congenital insensitivity to pain with anhidrosis (CIPA) Congenital pulmonary airway malformation (CPAM) Conjoined twins; Costello syndrome; Craniopagus parasiticus; Cri du chat syndrome; Cyclopia; Cystic fibrosis
The DSM-IV-TR contains expanded descriptions of disorders. Wordings were clarified and errors were corrected. The categorizations and the diagnostic criteria were largely unchanged. No new disorders or conditions were introduced, although a small number of subtypes were added and removed.
Diagnosis is based on an assessment of growth, facial features, central nervous system, and alcohol exposure by a multi-disciplinary team of professionals. The main criteria for diagnosis of FASD is nervous system damage and alcohol exposure, with FAS including congenital malformations of the lips and growth deficiency.
Pages in category "Neurological disorders in children" The following 40 pages are in this category, out of 40 total. This list may not reflect recent changes .
Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop. [4] If one parent has neurofibromatosis, his or her children have a 50% chance of developing the condition as well.