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Warburg Micro syndrome
* rare autosomal recessive genetic disorder.
- characterized by problems with the eyes and with the growth and development of the brain, resulting in neurodevelopmental delay.
- severe intellectual disability, microcephaly, hypothalamic hypogonadism
- mutations in at least four different genes, RAB18, RAB3GAP1, RAB3GAP2, or TCB1D20, causes this disorder
- in 1993 Warburg used the term MICRO syndrome to describe an autosomal recessive syndrome comprising Microcephaly, Microcornea, congenital Cataract, mental Retardation, Optic atrophy, and hypogenitalism
- the disorder is part of a spectrum of disease that includes Martsolf syndrome at the mild end, and linked to mutations in RAB3GAP2.
Differential diagnosis
Discussion