Dyggve-Melchior-Clausen disease (Q88337): Difference between revisions
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Doença de Dyggve-Melchior-Clausen é um transtorno esquelético raro pertencente ao grupo das displasias espondiloepimetafisárias (SEMD), e caracterizada por nanismo progressivo com tronco curto, esterno protuberante, microcefalia e incapacidade intelectual de gravidade variável. | |||
| description / en | description / en | ||
Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity. | |||
Revision as of 14:32, 15 August 2026
Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_21266164 |
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| English | Dyggve-Melchior-Clausen disease |
Dyggve-Melchior-Clausen disease is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias (SEMD), and characterised by progressive dwarfism with short trunk, protruding sternum, microcephaly and mental retardation of varying severity. |
