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  • Title: A 45,XX,-5,-14,+t(5q;14q)mat cri du chat child.
    Author: Bass HN, Sparkes RS, Crandall BF, Galos KJ, Howard J.
    Journal: Ann Genet; 1978 Mar; 21(1):56-9. PubMed ID: 308345.
    Abstract:
    A two-year-old girl has the following features of the cri du chat syndrome: microcephaly, hypertelorism, downward slanting of the palpebral fissures, psychomotor retardation and a cat-like cry. She is only of five patients having the cat cry syndrome with 45 chromosomes. Her karyotype is 45,XX, -5, -14, +t(5; 14)(5qter leads to 5p11: : 14q11 leads to 14qter) with the translocation inherited from her mother and maternal grandmother, each of whom is the carrier of a balanced translocation 46,XX,t(5;14)(p11q11). Normal plasma activity for hexosaminidase B suggests the locus for this enzyme is not located in the delected segment of 5 p.
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