Achondrogenesis type 1A (Q64674): Difference between revisions
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Acondrogenesia tipo 1A, uma forma de acondrogesia, é uma displasia esquelética letal muito rara caracterizada por nanismo com membros extremamente curtos, tórax estreito, costelas curtas que fraturam facilmente, ossos do crânio moles e características histológicas distintas da cartilagem. | |||
| description / en | description / en | ||
Achondrogenesis type 1A, a form of achondrogenesis, is a very rare, lethal skeletal dysplasia characterised by dwarfism with extremely short limbs, narrow chest, short ribs that are easily fractured, soft skull bones and distinctive histological features of the cartilage. | |||
Revision as of 12:23, 14 August 2026
Achondrogenesis type 1A, a form of achondrogenesis, is a very rare, lethal skeletal dysplasia characterised by dwarfism with extremely short limbs, narrow chest, short ribs that are easily fractured, soft skull bones and distinctive histological features of the cartilage.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1984401402 |
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| English | Achondrogenesis type 1A |
Achondrogenesis type 1A, a form of achondrogenesis, is a very rare, lethal skeletal dysplasia characterised by dwarfism with extremely short limbs, narrow chest, short ribs that are easily fractured, soft skull bones and distinctive histological features of the cartilage. |
