Warburg micro syndrome in two children from a highly inbred Turkish family

Genetic Counseling

Volumn 23, Issue 2, 2012, Pages 169-174

  Yildirim, M Selman ^a   Zamani, A G ^a   Bozkurt, B ^b  

^a NECMETTIN ERBAKAN UNIVERSITY   (Turkey)

^b SELCUK UNIVERSITY   (Turkey)

Author keywords

Cataract; Consanguinity; Micro syndrome

Indexed keywords

ACUTE SCROTUM; ARTICLE; BLADDER DIVERTICULUM; BRAIN ATROPHY; BRAIN VENTRICLE DILATATION; CASE REPORT; CHILD; CHILDHOOD DISEASE; CONGENITAL CATARACT; CONGENITAL HYPOTHYROIDISM; CONSANGUINITY; CRYPTORCHISM; ECHOGRAPHY; FACE DYSMORPHIA; FEMALE; GENETIC ASSOCIATION; GROWTH RETARDATION; HUMAN; HYPERTRICHOSIS; INFANTILE HYPOTONIA; MALE; MICROCEPHALY; MICROPENIS; MICROPHTHALMIA; MUSCLE CONTRACTURE; NUCLEAR MAGNETIC RESONANCE IMAGING; OBESITY; OPTIC NERVE ATROPHY; PHENOTYPE; PRESCHOOL CHILD; PSYCHOMOTOR RETARDATION; PTOSIS; URETER DILATATION; WALKER WARBURG SYNDROME; WARBURG MICRO SYNDROME;

ABNORMALITIES, MULTIPLE; CATARACT; CHILD, PRESCHOOL; CONSANGUINITY; CORNEA; FEMALE; HUMANS; HYPOGONADISM; INFANT; INTELLECTUAL DISABILITY; MALE; MICROCEPHALY; OPTIC ATROPHY; PEDIGREE; RAB3 GTP-BINDING PROTEINS; TURKEY;

EID: 84864459541     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

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