Partial Distal 10q Trisomy Due to De Novo Amplification: A new Case Without Furrows or Ridges in Fingers and Palms

Authors

  • Aliakbar Rahbarimanesh Bahrami hospital, Medical Sciences/University of Tehran, Iran, PO Box 14155-1595
  • Amirhassan Barkhordari Bahrami hospital, Medical Sciences/University of Tehran, Iran, PO Box 14155-1595
  • Pupak Derakhshandeh-Peykar Bahrami hospital, Medical Sciences/University of Tehran, Iran, PO Box 14155-1595-Department of Medical Genetics, Medical Sciences/University of Tehran, Iran, PO Box 14155-1595-Medizinisch Genetisches Zentrum (MGZ), Munich, Germany, P.O. Box 201412
  • Reza Ebrahimzadeh-Vesal Department of Medical Genetics, Medical Sciences/University of Tehran, Iran, PO Box 14155-1595
  • Soja Shamizadeh Kalkhoran Bahrami hospital, Medical Sciences/University of Tehran, Iran, PO Box 14155-1595
Abstract:

Background: Here we describe a new case of partial distal 10q trisomy in a 6-year-old Iranian girl from healthy parents with mental, growth, and psychomotor retardations. Methods: Additional clinical features include dysmorphic craniofacial features, microcephaly, bilateral hydronephrosis without heart problems, small and rotated low-set ears, bow-shaped mouth, abnormal teeth, short neck, and as a first case reported, fingers with camptodactly (i.e., without any furrows or ridges in the palms and fingers). Results: Cytogenetic analysis (GTG-banding) revealed an unbalanced female karyotype with additional bands at the end of the long arm of chromosome 10, karyotype: 46,XX,dup(10)(q25q26). Conclusion: According to the banding pattern it is most likely that a duplication of the distal part of the long arm of chromosome 10 occurred.

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Journal title

volume 1  issue 2

pages  87- 90

publication date 2013-05

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