Recognition of Zellweger syndrome in infancy

Advances in Neonatal Care

Volumn 5, Issue 1, 2005, Pages 5-13

  Grayer, Jennifer ^a  

^a The Women's Hospital of Greensboro   (United States)

Author keywords

Cerebro hepato renal disease; Infant; Metabolic disorders; Neuronal migration disorders; Newborn; Peroxisomal biogenesis disorders; Peroxisomal dysfunction; Peroxisomes; Physical assessment; Zellweger syndrome

Indexed keywords

ANTICONVULSIVE AGENT; FURETHIDINE; STEROID; URSODEOXYCHOLIC ACID;

ADRENAL DISEASE; BRAIN DEVELOPMENT; CELL MIGRATION; CENTRAL NERVOUS SYSTEM; CHEMICAL ANALYSIS; CLINICAL FEATURE; DIET SUPPLEMENTATION; DIFFERENTIAL DIAGNOSIS; GENETIC COUNSELING; HUMAN; INFANCY; LIVER INJURY; METABOLIC DISORDER; MICROGYRIA; NERVE CELL; NERVOUS SYSTEM DEVELOPMENT; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; NURSING; PEROXISOME; PHYSICAL EXAMINATION; PRENATAL SCREENING; QUALITY OF LIFE; REVIEW; SEIZURE; VITAMIN SUPPLEMENTATION; ZELLWEGER SYNDROME;

BRAIN; BRAIN DISEASES, METABOLIC; FEMALE; HUMANS; INFANT; MALE; MUSCLE HYPOTONIA; MUSCLES; PEDIGREE; PEROXISOMES; SKIN; ZELLWEGER SYNDROME;

EID: 15944368116     PISSN: 15360903     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.adnc.2004.10.007     Document Type: Review

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