2p15-16.1 microdeletion syndrome

2p15-16.1 Microdeletion Syndrome

High resolution image of human chromosome 2.

Diagram of chromosome 2.

2p15-16.1 microdeletion syndrome is a rare genetic disorder caused by a deletion of a small segment of chromosome 2. This condition is characterized by a variety of clinical features, which can include developmental delay, intellectual disability, and distinctive facial features.

Genetic Basis

The syndrome is caused by a microdeletion on the short arm of chromosome 2, specifically in the region designated as 2p15-16.1. This deletion results in the loss of several genes, which are believed to contribute to the clinical manifestations of the syndrome. The exact size of the deletion can vary among affected individuals, leading to a range of phenotypic expressions.

Clinical Features

Individuals with 2p15-16.1 microdeletion syndrome often present with:

• Developmental delay
• Intellectual disability
• Distinctive facial features such as a broad forehead, hypertelorism (wide-set eyes), and a short nose
• Microcephaly (small head size)
• Hypotonia (reduced muscle tone)

Diagnosis

Diagnosis of 2p15-16.1 microdeletion syndrome is typically made through genetic testing, such as chromosomal microarray analysis or fluorescence in situ hybridization (FISH), which can detect the specific deletion on chromosome 2.

Management

There is no cure for 2p15-16.1 microdeletion syndrome, and treatment is focused on managing the symptoms and providing supportive care. This may include:

• Early intervention programs for developmental delays
• Special education services
• Physical and occupational therapy
• Regular monitoring by a team of specialists

Related Pages

• Chromosome 2
• Microdeletion syndrome
• Genetic disorder
• Developmental delay

Gallery

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  High resolution image of human chromosome 2.
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  Diagram of chromosome 2.

2p15-16.1 microdeletion syndrome

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  Human male karyotype high resolution - Chromosome 2
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  Chromosome 2