TY  - JOUR
T1  - 4Q- syndrome
AU  - Townes PL, White M, Di Marzo SV
Y1  - 1979/04/01
N1  - 10.1001/archpedi.1979.02130040037008
JO  - American Journal of Diseases of Children
SP  - 383
EP  - 385
VL  - 133
IS  - 4
N2  - • To our knowledge, there have been three prior reports of patients found, with trypsin-Giemsa banding, to be monosomic for the terminal q segment of chromosome 4. Described herein is a fourth patient with this chromosome abnormality. Comparison of these four patients suggests a characteristic phenotype in the 4q- syndrome: cleft palate, satyr deformity of the pinnae, snub nose, retrognathia and micrognathia, hypertelorism, oropharyngeal hypotonia or upper airway obstruction, cardiac defect, clinodactyly of the fifth fingers with absence of a flexion crease, simian lines, displaced or clinodactylous toes, and mental retardation. In the three prior reports, the 4q-syndrome resulted from a de novo deletion. In the present case, the 4q monosomy was inherited from the father, who had a 4;20 translocation.(Am J Dis Child 133:383-385, 1979)
SN  - 0002-922X
M3  - doi: 10.1001/archpedi.1979.02130040037008
UR  - http://dx.doi.org/10.1001/archpedi.1979.02130040037008
ER  -