Case Reports
Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome
- PMID: 6674417
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Case Reports
Del (8) (q212q2200) de novo in a boy without Langer-Giedion syndrome
J Genet Hum.
1983 Dec.
Abstract
A two year-old boy with congenital malformations, psychomotor retardation and absence of phenotypical features of the Langer-Giedion syndrome (LGS) was found to have a de novo del (8) (q212q2200). The comparative analysis with other 8q monosomic cases suggests the existence of at least two distinct syndromes: one due to the monosomy of a part of the segment 8q22----q24, clinically manifested as the LGS, and the other to the deletion of the band 8q21.
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