Lenz–Majewski syndrome
Lenz-Majewski hyperostotic dwarfism is an extremely rare syndrome associating dwarfism, characteristic facial appearance, cutis laxa and progressive bone sclerosis
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Lenz–Majewski syndrome
Summary
Lenz–Majewski syndrome is a developmental defect during embryogenesis[1]. It draws 72 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2]
Key Facts
- Lenz–Majewski syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Lenz–Majewski syndrome's instance of is recorded as rare disease[4].
- Lenz–Majewski syndrome's instance of is recorded as class of disease[5].
- Lenz–Majewski syndrome is a type of dwarfism[6].
- Lenz–Majewski syndrome is a type of primary bone dysplasia with increased bone density[7].
- Lenz–Majewski syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Lenz–Majewski syndrome is a type of genetic syndromic intellectual disability[9].
- Lenz–Majewski syndrome's health specialty is recorded as medical genetics[10].
- Lenz–Majewski syndrome's genetic association is recorded as PTDSS1[11].
- Lenz–Majewski syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2658[12].
Why It Matters
Lenz–Majewski syndrome draws 72 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #134 of 308).[2] It is known by 16 alternative names across languages and contexts.[13]