1. Mendelian
  2. Rare Diseases
  3. MOMO SYNDROME

Momo Syndrome

Table of contents:

Description

MOMO syndrome is a very rare genetic overgrowth/obesity syndrome (see this term) 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.

Clinical Features

Top most frequent phenotypes and symptoms related to Momo Syndrome

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Hypertelorism
  • Nystagmus
  • Strabismus
  • High palate
  • Delayed speech and language development

And another 50 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Momo Syndrome Is also known as macrocephaly-obesity-mental disability-ocular abnormalities syndrome, macrosomia, obesity, macrocephaly, and ocular abnormalities, macrosomia-obesity-macrocephaly-ocular abnormalities syndrome.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Sources and references

You can check the following sources for additional information.

OMIM MESH ORPHANET Rare Disease Search Engine

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