Raine syndrome
Lethal osteosclerotic bone dysplasia is defined by generalized osteosclerosis with periosteal bone formation, characteristic facial dysmorphism, brain abnormalities including intracerebral calcifications, and neonatal lethal course
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Raine syndrome
Summary
Raine syndrome is a developmental defect during embryogenesis[1]. It draws 91 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #118 of 308).[2]
Key Facts
- Raine syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Raine syndrome's instance of is recorded as rare disease[4].
- Raine syndrome's instance of is recorded as class of disease[5].
- Raine syndrome is a type of bone disease[6].
- Raine syndrome is a type of neonatal osteosclerotic dysplasia[7].
- Raine syndrome's genetic association is recorded as FAM20C[8].
- Raine syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1832[9].
Why It Matters
Raine syndrome draws 91 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #118 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[10] It is known by 9 alternative names across languages and contexts.[11]