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Learn About Chromosome 7p Deletion

What is the definition of Chromosome 7p Deletion?
Chromosome 7p 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 7. 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 7p 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 7p Deletion?
  • Chromosome 7p deletion
  • 7p deletion
  • 7p monosomy
  • Deletion 7p
  • Monosomy 7p
  • Partial monosomy 7p
Who are the top Chromosome 7p Deletion Local Doctors?
Elite in Chromosome 7p Deletion
Elite in Chromosome 7p Deletion
Robert Koch Str. 40, 
Goettingen, NI, DE 

Detlef Haase practices in Goettingen, Germany. Haase is rated as an Elite expert by MediFind in the treatment of Chromosome 7p Deletion. Their top areas of expertise are Myelodysplastic Syndrome (MDS), Chromosome 7p Deletion, Acute Myeloid Leukemia (AML), Vitrectomy, and Bone Marrow Transplant.

Elite in Chromosome 7p Deletion
Elite in Chromosome 7p Deletion
Hiroshima, JP 

Toshiya Inaba practices in Hiroshima, Japan. Inaba is rated as an Elite expert by MediFind in the treatment of Chromosome 7p Deletion. Their top areas of expertise are Chromosome 7p Deletion, Leukemia, Myelodysplastic Syndrome (MDS), and Acute Lymphoblastic Leukemia (ALL).

 
 
 
 
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Elite in Chromosome 7p Deletion
Elite in Chromosome 7p Deletion
Munich, BY, DE 

Torsten Haferlach practices in Munich, Germany. Mr. Haferlach is rated as an Elite expert by MediFind in the treatment of Chromosome 7p Deletion. His top areas of expertise are Leukemia, Acute Myeloid Leukemia (AML), Myelodysplastic Syndrome (MDS), RUNX1 Familial Platelet Disorder, and Bone Marrow Transplant.

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