Michels Caskey syndrome

Michels Caskey syndrome is a rare genetic disorder characterized by a combination of congenital anomalies and developmental delays. The syndrome is named after the researchers who first described it, Dr. Michels and Dr. Caskey.

Clinical Features

Individuals with Michels Caskey syndrome typically present with a variety of clinical features, which may include:

• Craniofacial abnormalities such as microcephaly, cleft palate, and hypertelorism.
• Cardiac anomalies including congenital heart defects.
• Skeletal abnormalities such as short stature and limb deformities.
• Neurological issues including developmental delay and intellectual disability.
• Ocular anomalies like strabismus and cataracts.

Genetics

Michels Caskey syndrome is believed to be inherited in an autosomal recessive manner. This means that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the disorder. The specific gene or genes involved in Michels Caskey syndrome have not yet been identified.

Diagnosis

The diagnosis of Michels Caskey syndrome is primarily based on clinical evaluation and the presence of characteristic features. Genetic testing may be used to confirm the diagnosis and to differentiate it from other syndromes with overlapping features.

Management

There is no cure for Michels Caskey syndrome, and treatment is primarily supportive and symptomatic. Management may involve a multidisciplinary team including:

• Pediatricians
• Cardiologists
• Neurologists
• Orthopedic surgeons
• Ophthalmologists
• Speech therapists
• Physical therapists

Prognosis

The prognosis for individuals with Michels Caskey syndrome varies depending on the severity of the symptoms and the presence of associated complications. Early intervention and supportive care can improve the quality of life for affected individuals.

See Also

• Congenital disorder
• Genetic disorder
• Developmental delay
• Craniofacial abnormalities
• Autosomal recessive inheritance

External Links

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