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Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome

✍ Scribed by K. R. Sandig; J. Mücke; H. Veit

Publisher
Springer
Year
1979
Tongue
English
Weight
576 KB
Volume
52
Category
Article
ISSN
0340-6717

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✦ Synopsis

Trisomy 9p with de novo 9/15 translocation and 9p isochromosome was observed in a mentally defective boy with typical clinical features for this syndrome. This chromosomal aberration is probably caused by the pericentric inversion of chromosome 9 of the patient's father.

📜 SIMILAR VOLUMES

Trisomy 9p resulting from maternal 9/21
Trisomy 9p resulting from maternal 9/21 translocation
✍ I. Šubrt; Bohunka Blehová; Blanka Pallová 📂 Article 📅 1976 🏛 Springer 🌐 English ⚖ 784 KB

The clinical picture found in a child with trisomy 9p confirmed that this chromosomal syndrome is a entity, which arises from maternal translocation t(9;21).

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The authors report on a young girl with generalized developmental deficits originally thought to be caused by an unusual reaction to DPT vaccination. At the age of 4(1/2) years, chromosome analysis showed that the terminus of the short arm of chromosome 9 had extra material believed to originate fro

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Case of partial trisomy 9p and partial trisomy 14q resulting from a maternal translocation: Overlapping manifestations of characteristic phenotypes
✍ Angle, Brad; Yen, Frank; Cole, Cameron W. 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 31 KB 👁 2 views

We report on a female infant with partial trisomy 9p (pter→p13) and partial trisomy 14q (pter→q22) resulting from a 3:1 segregation of a maternal reciprocal translocation (9;14)(p13;q22). Both trisomy 9p and partial trisomy 14q have been described as recognized phenotypes with characteristic pattern