MOMO syndrome
extremely rare genetic disorder which belongs to the overgrowth syndromes and has been diagnosed in only six cases around the world, and occurs in 1 in 100 million births
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MOMO syndrome
Summary
MOMO syndrome is a rare disease[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- MOMO syndrome's instance of is recorded as rare disease[3].
- MOMO syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- MOMO syndrome's instance of is recorded as class of disease[5].
- MOMO syndrome is a type of syndromic obesity[6].
- MOMO syndrome's symptoms and signs is recorded as obesity[7].
- MOMO syndrome's symptoms and signs is recorded as macrocephaly[8].
- MOMO syndrome's symptoms and signs is recorded as intellectual disability[9].
- MOMO syndrome's symptoms and signs is recorded as eye disease[10].
- MOMO syndrome's health specialty is recorded as genetics[11].
Why It Matters
MOMO syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[12]