Tuesday, August 30, 2011

Some general information on missing Chromosome 2 (2q37 Deletion Syndrome)

Although Victoria does not fit into all of the symptoms listed below, she does have a lot of them... It did state that 2q37 deletion syndrome appears to be a rare condition, although its exact prevalence is unknown. Approximately 100 cases have been reported worldwide.


What is 2q37 deletion syndrome?

2q37 deletion syndrome is a condition that can affect many parts of the body. This condition is characterized by weak muscle tone (hypotonia) in infancy, mild to severe intellectual disability and developmental delay, behavioral problems, characteristic facial features, and other physical abnormalities.
Most babies with 2q37 deletion syndrome are born with hypotonia, which usually improves with age. About 25 percent of people with this condition have autism, a developmental condition that affects communication and social interaction.
The characteristic facial features associated with 2q37 deletion syndrome include a prominent forehead, highly arched eyebrows, deep-set eyes, a flat nasal bridge, a thin upper lip, and minor ear abnormalities. Other features of this condition can include short stature, obesity, unusually short fingers and toes (brachymetaphalangy), sparse hair, heart defects, seizures, and an inflammatory skin disorder called eczema. A few people with 2q37 deletion syndrome have a rare form of kidney cancer called Wilms tumor. Some affected individuals have malformations of the brain, gastrointestinal system, kidneys, and/or genitalia.

How common is 2q37 deletion syndrome?

2q37 deletion syndrome appears to be a rare condition, although its exact prevalence is unknown. Approximately 100 cases have been reported worldwide.

What are the genetic changes related to 2q37 deletion syndrome?

2q37 deletion syndrome is caused by a deletion of genetic material from a specific region in the long (q) arm of chromosome 2. The deletion occurs near the end of the chromosome at a location designated 2q37. The size of the deletion varies among affected individuals. The signs and symptoms of this disorder are probably related to the loss of multiple genes in this region.
Read more about chromosome 2.

Can 2q37 deletion syndrome be inherited?

Most cases of 2q37 deletion syndrome are not inherited. They result from a chromosomal deletion that occurs as a random event during the formation of reproductive cells (eggs or sperm) or in early fetal development. Affected people typically have no history of the disorder in their family.
Rarely, affected individuals inherit a copy of chromosome 2 with a deleted segment from an unaffected parent. In these cases, one of the parents carries a chromosomal rearrangement between chromosome 2 and another chromosome. This rearrangement is called a balanced translocation. No genetic material is gained or lost in a balanced translocation, so these chromosomal changes usually do not cause any health problems. However, translocations can become unbalanced as they are passed to the next generation. Children who inherit an unbalanced translocation can have a chromosomal rearrangement with extra or missing genetic material. Some individuals with 2q37 deletion syndrome inherit an unbalanced translocation that deletes genetic material near the end of the long arm of chromosome 2, which results in birth defects and other health problems characteristic of this disorder.

Where can I find information about diagnosis, management, or treatment of 2q37 deletion syndrome?

These resources address the diagnosis or management of 2q37 deletion syndrome and may include treatment providers.
You might also find information on the diagnosis or management of 2q37 deletion syndrome in Educational resources and Patient support.
To locate a healthcare provider, see How can I find a genetics professional in my area? in the Handbook.

Where can I find additional information about 2q37 deletion syndrome?

You may find the following resources about 2q37 deletion syndrome helpful. These materials are written for the general public.
You may also be interested in these resources, which are designed for healthcare professionals and researchers.

What other names do people use for 2q37 deletion syndrome?

  • Albright hereditary osteodystrophy-like syndrome
  • brachydactyly-mental retardation syndrome
For more information about naming genetic conditions, see the Genetics Home Reference Condition Naming Guidelines and How are genetic conditions and genes named? in the Handbook.

What if I still have specific questions about 2q37 deletion syndrome?

Where can I find general information about genetic conditions?

What glossary definitions help with understanding 2q37 deletion syndrome?

References (5 links)

The resources on this site should not be used as a substitute for professional medical care or advice. Users seeking information about a personal genetic disease, syndrome, or condition should consult with a qualified healthcare professional. See How can I find a genetics professional in my area? in the Handbook.

1 comment:

  1. Hi Denise! I stumbled onto your blog by researching info-you have done some great summarizing! I was actually thinking of doing some for my friends and family. My 6 year old was just diagnosed with a chromosome 2 deletion and I too started a blog that until today have kept personal because it's like a journal and I used it to "vent". She has been a mystery until a couple weeks ago. I was happy to see this:) I would love to know any more findings you come across and here is a link to mine...good luck:)