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Archives of Pediatrics and Adolescent Medicine

Volumn 153, Issue 10, 1999, Pages 1105-1106

  Dana, Jalal Rais ^a,c   Tunnessen Jr , Walter W ^b  

^a Sinai First   (United States)

^b AMERICAN BOARD OF PEDIATRICS   (United States)

^c NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; HUMAN; INFANT; MUSCLE HYPOTONIA; PRIORITY JOURNAL; SUCKING; WEIGHT REDUCTION; ZELLWEGER SYNDROME; CONSANGUINITY; GENETICS; PATHOPHYSIOLOGY; PROGNOSIS; REVIEW;

CONSANGUINITY; HUMANS; INFANT; PROGNOSIS; ZELLWEGER SYNDROME;

EID: 0032873669     PISSN: 10724710     EISSN: None     Source Type: Journal    
DOI: 10.1001/archpedi.153.10.1105     Document Type: Article

References (7)

1. Bowen P, Lee CSN, Zellweger H, Lindberg R. A familial syndrome of multiple congenital defects. Bull Johns Hopkins Hosp. 1964;114:402-414.
2. Smith DW, Opitz JM, Inhorn SL. A syndrome of multiple developmental defects including polycystic kidney disease and intrahepatic biliary dysgenesis in two siblings. J Peaiatr. 1965;67:617-624.
3. Goldfischer S, Moore CL, Johnson AB, et al. Peroxisomal and mitochondrial defects in the cerebrohepatorenal disease. Science, 1973;182:62-64.
4. Kamei A, Houdou S, Takashima S, Suzuki Y, Becker LE, Armstrong DL. Peroxisomal disorders in children: immunohistochemistry and neuropathology. J Pediatr. 1993;122:573-579.
5. Moser AB, Rasmussen M, Naidu S, et al. Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups. J Pediatr. 1995; 127:13-22.
6. Aikawa J, Sato K, Miyabayashi S, et al. Prenatal diagnosis in high risk pregnancies for Zellweger syndrome. Acta Paediatr Jpn. 1992;34:454-458.
7. Theil AC, Schutgens RBH, Wanders RJA, Heymans HSA. Clinical recognition of patients affected by a peroxisomal disorder: a retrospective study in 40 patients. Eur J Pediatr. 1992;151:117-120.