Wolf Syndrome (Monosomy 4 Partial Syndrome; Chromosome
4 Partial Deletion Syndrome;
Hirschhorn-Cooper Syndrome) 252f52c 252f52c 252f52c 252f52c 252f52c 1
General: Partial deletion of chromosome 4 of the B group; short life expectancy; present from birth (see Cri-du-Chat Syndrome).
Ocular: Hypertelorism; antimongoloid slanting of palpebral fissures; ptosis; nystagmus;strabismus; iris coloboma; retinal coloboma.
Clinical: Microcephaly; mental retardation; seizures; ear malformations; hypospadias; beaked nose; broad nasal root; cleft lip and palate; hypotonia.
Pau H. Differential diagnosis of eye diseases. New York: Thieme, 1987.
Wolf U, et al. Deletion on short arms of a B-chromosome without cri-du-chat syndrome. Lancet 1965; 1:769.
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