MOMO syndrome

MONDO:0008008

MOMO syndrome is a very rare genetic overgrowth/obesity syndrome characterized by macrocephaly, obesity, mental (intellectual) disability and ocular abnormalities. Other frequent clinical signs include macrosomia, downslanting palpebral fissures, hypertelorism, broad nasal root, high and broad forehead and delay in bone maturation, in association with normal thyroid function and karyotype.

Also known as: MOMO syndrome, macrocephaly-obesity-mental disability-ocular abnormalities syndrome, macrosomia-obesity-macrocephaly-ocular abnormalities syndrome, macrocrania, obesity, ocular abnormalities (retinal coloboma and nystagmus), macrosomia, obesity, macrocephaly, and ocular abnormalities, macrosomia, obesity, macrocephaly, ocular abnormalities

0 clinical trials for this condition and its sub-types, 0 tagged with MOMO syndrome itself.

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