Lubani Al Saleh Teebi syndrome
Lubani Al Saleh Teebi syndrome is a rare genetic disorder characterized by a variety of physical and developmental abnormalities. It was first described by Dr. Lubani and Dr. Al Saleh Teebi, hence the name.
Symptoms and Signs[edit | edit source]
The syndrome is characterized by a number of symptoms, including microcephaly (small head size), intellectual disability, growth retardation, and distinctive facial features. Other symptoms may include hypotonia (low muscle tone), seizures, and congenital heart defects.
Causes[edit | edit source]
Lubani Al Saleh Teebi syndrome is a genetic disorder, which means it is caused by abnormalities in the individual's genes. It is believed to be inherited in an autosomal recessive manner, which means both parents must carry a copy of the mutated gene for a child to be affected.
Diagnosis[edit | edit source]
Diagnosis of Lubani Al Saleh Teebi syndrome is typically based on the presence of characteristic clinical features. Genetic testing may also be used to confirm the diagnosis and identify the specific gene mutation.
Treatment[edit | edit source]
There is currently no cure for Lubani Al Saleh Teebi syndrome. Treatment is symptomatic and supportive, and may include physical therapy, special education, and medication for seizures.
Prognosis[edit | edit source]
The prognosis for individuals with Lubani Al Saleh Teebi syndrome varies depending on the severity of symptoms. Some individuals may have a normal lifespan, while others may have life-threatening complications.
See Also[edit | edit source]
NIH genetic and rare disease info[edit source]
Lubani Al Saleh Teebi syndrome is a rare disease.
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