Adolescent presentations of inborn errors of metabolism

Journal of Adolescent Health

Volumn 56, Issue 5, 2015, Pages 477-482

  Ahrens Nicklas, Rebecca C ^a   Slap, Gail ^a   Ficicioglu, Can ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Adolescent health services; Fatty acid oxidation complex; Inborn errors metabolism; Mitochondrial diseases; Neonatal screening; Urea cycle disorders

Indexed keywords

ACUTE DISEASE; ADOLESCENT DISEASE; AVOIDANCE BEHAVIOR; CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY; FAILURE TO THRIVE; FAMILY HISTORY; FATTY ACID OXIDATION; GENERAL PRACTITIONER; HUMAN; INBORN ERROR OF METABOLISM; MEDICAL HISTORY; MELAS SYNDROME; NEWBORN SCREENING; ORNITHINE TRANSCARBAMYLASE DEFICIENCY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; REVIEW; UREA CYCLE; ADOLESCENT; ANAMNESIS; EARLY DIAGNOSIS; METABOLISM, INBORN ERRORS; PATHOPHYSIOLOGY;

ADOLESCENT; EARLY DIAGNOSIS; HUMANS; MEDICAL HISTORY TAKING; METABOLISM, INBORN ERRORS; PHYSICAL EXAMINATION; PHYSICIANS, PRIMARY CARE;

EID: 84928017611     PISSN: 1054139X     EISSN: 18791972     Source Type: Journal    
DOI: 10.1016/j.jadohealth.2015.01.008     Document Type: Review

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