Neonatal progeroid syndrome (Wiedemann-Rautenstrauch syndrome) in an Egyptian child with premature loss of teeth, and café au lait skin patches

Egyptian Journal of Medical Human Genetics

Volumn 13, Issue 2, 2012, Pages 227-231

  Shawky, Rabah M ^a   Abd Elkhalek, Heba Salah ^a   Gad, Shimaa ^a   Seifeldin, Neveen S ^a  

^a AIN SHAMS UNIVERSITY   (Egypt)

Author keywords

Caf au lait skin patches; Milk teeth; Nail dystrophy; Premature aging; The neonatal progeroid syndrome; Wiedemann Rautenstrauch syndrome

Indexed keywords

CHOLESTEROL; TRIACYLGLYCEROL;

ARTICLE; CAFE AU LAIT SPOT; CASE REPORT; CHILD; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; FEMALE; GENETIC DISORDER; GROWTH DISORDER; HUMAN; HYDROCEPHALUS; HYPERCHOLESTEROLEMIA; LIPOATROPHY; MENTAL DEFICIENCY; NAIL DYSTROPHY; NEONATAL PROGEROID SYNDROME; NEUROIMAGING; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PHYSICAL EXAMINATION; PREMATURE AGING; PREMATURE LOSS OF TEETH; PRESCHOOL CHILD; PROGERIA; PSEUDOHYDROCEPHALUS; TOOTH DISEASE; WIEDEMANN RAUTENSTRAUCH SYNDROME;

EID: 84900372971     PISSN: 11108630     EISSN: 20902441     Source Type: Journal    
DOI: 10.1016/j.ejmhg.2012.03.008     Document Type: Article

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