Chromosome 10q Deletion Overview

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Learn About Chromosome 10q Deletion

What is the definition of Chromosome 10q Deletion?
Chromosome 10q deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the long arm (q) of chromosome 10. The severity of the condition and the signs and symptoms depend on the size and location of the deletion and which genes are involved. Features that often occur in people with Chromosome 10q deletion include developmental delay, intellectual disability, behavioral problems, and distinctive facial features. Most cases are not inherited, but people can pass the deletion on to their children.
What are the alternative names for Chromosome 10q Deletion?
  • Chromosome 10q deletion
  • 10q deletion
  • 10q monosomy
  • Deletion 10q
  • Monosomy 10q
  • Partial monosomy 10q
Who are the top Chromosome 10q Deletion Local Doctors?
Distinguished in Chromosome 10q Deletion
Akito Sutani
Distinguished in Chromosome 10q Deletion
Akito Sutani
Kawaguchi, JP 

Akito Sutani practices in Kawaguchi, Japan. Mr. Sutani is rated as a Distinguished expert by MediFind in the treatment of Chromosome 10q Deletion. His top areas of expertise are Chromosome 10q Deletion, Retropharyngeal Abscess, Renal Glycosuria, Bone Marrow Transplant, and Hormone Replacement Therapy (HRT).

Distinguished in Chromosome 10q Deletion
Melanie Lacaria
Distinguished in Chromosome 10q Deletion
Melanie Lacaria
Ottawa, ON, CA 

Melanie Lacaria practices in Ottawa, Canada. Ms. Lacaria is rated as a Distinguished expert by MediFind in the treatment of Chromosome 10q Deletion. Her top areas of expertise are Chromosome 10q Deletion, Primary Lateral Sclerosis, Mitochondrial Complex 1 Deficiency, and Drug Induced Dyskinesia.

 
 
 
 
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Experienced in Chromosome 10q Deletion
Dr. Staci Kallish
Medical Genetics
Experienced in Chromosome 10q Deletion
Dr. Staci Kallish
Medical Genetics

Penn Translational Medicine And Human Genetics

3400 Civic Center Boulevard, South Pavilion, 1st Floor, 
Philadelphia, PA 
800-789-7366
Languages Spoken:
English
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Accepting New Patients
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Staci Kallish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kallish is rated as an Experienced provider by MediFind in the treatment of Chromosome 10q Deletion. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Gaucher Disease Type 1, Fabry Disease, and Neurofibromatosis. Dr. Kallish is currently accepting new patients.

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Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center