Craniomicromelic syndrome (Q93981): Difference between revisions
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Revision as of 09:05, 16 August 2026
Craniomicromelic syndrome is a very rare skeletal disorder characterised by intrauterine growth retardation, under ossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly. Dysmorphic features include narrow face with small palpebral fissures, small pointed nose, microstomia, micrognathia and low-set and posteriorly rotated ears.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1734157428 |
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| English | Craniomicromelic syndrome |
Craniomicromelic syndrome is a very rare skeletal disorder characterised by intrauterine growth retardation, under ossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly. Dysmorphic features include narrow face with small palpebral fissures, small pointed nose, microstomia, micrognathia and low-set and posteriorly rotated ears. |
Statements
CID11:ID_1734157428
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