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Learn About Chromosome 4p Deletion

What is the definition of Chromosome 4p Deletion?
Chromosome 4p deletion is a chromosome abnormality that occurs when there is a missing copy of the genetic material located on the short arm (p) of chromosome 4. 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 4p 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 4p Deletion?
  • Chromosome 4p deletion
  • 4p deletion
  • 4p monosomy
  • Deletion 4p
  • Monosomy 4p
  • Partial monosomy 4p
Who are the top Chromosome 4p Deletion Local Doctors?
Distinguished in Chromosome 4p Deletion
Distinguished in Chromosome 4p Deletion
Belgrade, SE, RS 

Tatjana Damnjanovic practices in Belgrade, Serbia. Ms. Damnjanovic is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4p Deletion. Her top areas of expertise are Chromosome 4p Deletion, Rheumatoid Arthritis (RA), Arthritis, and Acrocephalopolydactyly.

Distinguished in Chromosome 4p Deletion
Distinguished in Chromosome 4p Deletion
Erciyes, TR 

Alper Ozcan practices in Erciyes, Turkey. Mr. Ozcan is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4p Deletion. His top areas of expertise are Scurvy, Chromosome 4p Deletion, Hemophagocytic Lymphohistiocytosis, Bone Marrow Aspiration, and Bone Marrow Transplant.

 
 
 
 
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Advanced in Chromosome 4p Deletion
Advanced in Chromosome 4p Deletion
Erciyes, TR 

Musa Karakukcu practices in Erciyes, Turkey. Mr. Karakukcu is rated as an Advanced expert by MediFind in the treatment of Chromosome 4p Deletion. His top areas of expertise are Infantile Neutropenia, Prothrombin Deficiency, Congenital Afibrinogenemia, Bone Marrow Transplant, and Synovectomy.

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