Lawrence-Muna-Bardé-Bidlya syndrome is a congenital symptom complex with obesity, underdevelopment of the genital organs, retinitis pigmentosa, mental retardation, growth retardation, polydactyly or syndactyly, deformities of the skull and skeleton, blockage of the anus, diabetes. In a syndrome, not all of these signs can be expressed.
The syndrome is based on congenital damage to the hypothalamic-pituitary area in the early stages of fetal development. The average life expectancy of patients 40 years.
The prognosis for vision is unfavorable.
Treatment of individual manifestations of the disease with hormonal drugs often causes some improvement in the condition.