Catel–Manzke syndrome
Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis
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Summary
Catel–Manzke syndrome is a head and neck disease[1]. It draws 21 Wikipedia views per month (head_and_neck_disease category, ranking #54 of 92).[2]
Key Facts
- Catel–Manzke syndrome's instance of is recorded as head and neck disease[3].
- Catel–Manzke syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Catel–Manzke syndrome's instance of is recorded as rare disease[5].
- Catel–Manzke syndrome's instance of is recorded as class of disease[6].
- Catel–Manzke syndrome is a type of Pierre Robin syndrome[7].
- Catel–Manzke syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Catel–Manzke syndrome is a type of orofacial clefting syndrome[9].
- Catel–Manzke syndrome is a type of genetic syndromic intellectual disability[10].
- Catel–Manzke syndrome is a type of syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[11].
- Catel–Manzke syndrome's genetic association is recorded as TGDS[12].
- Catel–Manzke syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1388[13].
Why It Matters
Catel–Manzke syndrome draws 21 Wikipedia views per month (head_and_neck_disease category, ranking #54 of 92).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[14] It is known by 14 alternative names across languages and contexts.[15]