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Duplication-deletion with Partial Trisomy Lq and Partial Monosomy 3p Resulting from a Maternal Reciprocal Translocation Rcp (1;3) (q32;p25)

Overview
Journal J Med Genet
Specialty Genetics
Date 1981 Feb 1
PMID 7253002
Citations 6
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Abstract

A mother with a translocation rcp (1;3) (q32;p25) gave birth to a son with duplication of 1q32 leads to qter and deletion of 3p25 leads to pter. At 17 1/2 years of age, the proband was severely mentally retarded and presented a pattern of multiple minor dysmorphic stigmata and anomalies, including hypertrichosis, synophrys, ocular hypertelorism, ptosis, convergent squint, cleft uvula nad narrow palate, poorly modelled auricles, funnel chest, kyphoscoliosis, umbilical and inguinal hernias, and cubitus valgus. He had normal stature and did not have any apparent malformations.

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References
1.
Yunis E, Egel H, Zuniga R, Ramirez E, Torres de Caballero O, Leibovici M . "De novo" trisomy 1q32 leads to 1qter and monosomy 3p25 leads to 3pter. Hum Genet. 1977; 36(1):113-6. DOI: 10.1007/BF00390442. View

2.
Steffensen D, Chu E, Speert D, Wall P, Meilinger K, Kelch R . Partial trisomy of the long arm of human chromosome 1 as demostrated by in situ hybridization with 5S ribosomal RNA. Hum Genet. 1977; 36(1):25-33. DOI: 10.1007/BF00390432. View

3.
Verjaal M, De Nef M . A patient with a partial deletion of the short arm of chromosome 3. Am J Dis Child. 1978; 132(1):43-5. DOI: 10.1001/archpedi.1978.02120260045012. View

4.
Fineman R, Hecht F, Ablow R, HOWARD R, BREG W . Chromosome 3 duplication q/deletion p syndrome. Pediatrics. 1978; 61(4):611-8. View

5.
Bourrouillou G, COLOMBIES P, Blanc P . [Secondary trisomy 1 q due to a reciprocal maternal translocation]. C R Seances Soc Biol Fil. 1978; 172(2):359-62. View