Chromosome 7, monosomy 7q2

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Chromosome 7, monosomy 7q2 is a rare chromosomal abnormality involving the deletion of the long arm (q arm) of chromosome 7 in the region designated as 7q2. This condition is characterized by a variety of clinical manifestations, which can include developmental delays, intellectual disabilities, physical abnormalities, and an increased risk of certain health conditions. The specific symptoms and severity can vary significantly among affected individuals, depending on the exact size and location of the deletion on chromosome 7.

Causes[edit | edit source]

Monosomy 7q2 results from a deletion of genetic material on the long arm of chromosome 7 at the q2 band. This deletion can occur randomly for unknown reasons (de novo) or can be inherited from a parent carrying a balanced chromosomal rearrangement, such as a translocation or inversion. The loss of genetic material disrupts normal development and can lead to the various clinical features associated with the condition.

Symptoms[edit | edit source]

The symptoms of Chromosome 7, monosomy 7q2 can vary widely but may include:

  • Developmental delay and intellectual disability
  • Growth abnormalities
  • Distinctive facial features
  • Skeletal anomalies
  • Heart defects
  • Kidney problems
  • Neurological issues

The severity and combination of symptoms can differ significantly from one individual to another.

Diagnosis[edit | edit source]

Diagnosis of Chromosome 7, monosomy 7q2 typically involves a combination of clinical evaluation and genetic testing. Karyotyping and fluorescence in situ hybridization (FISH) can be used to identify the chromosomal deletion. More recently, array comparative genomic hybridization (aCGH) and next-generation sequencing technologies have provided more detailed information about the size and extent of the deletion.

Treatment[edit | edit source]

There is no cure for Chromosome 7, monosomy 7q2, and treatment is symptomatic and supportive. Management may include:

  • Early intervention programs for developmental delays
  • Educational support
  • Physical therapy
  • Speech therapy
  • Occupational therapy
  • Regular monitoring and treatment for any associated health issues, such as heart or kidney problems

Prognosis[edit | edit source]

The prognosis for individuals with Chromosome 7, monosomy 7q2 varies depending on the severity of symptoms and the presence of associated health conditions. Early intervention and supportive care can improve the quality of life and outcomes for many affected individuals.

See also[edit | edit source]

Chromosome 7, monosomy 7q2 Resources
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Contributors: Prab R. Tumpati, MD