acromicric dysplasia
MeSH: C535662ORPHA: 969
Overview
Acromicric dysplasia is a rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with acromicric dysplasia, sourced from HPO and Orphanet clinical annotations.
Narrow mouthThick lower lip vermilionRound faceLong philtrumBulbous noseAnteverted naresLong eyelashesAbnormal eyebrow morphologyDecreased nerve conduction velocityBrachydactylyJoint stiffnessHoarse voiceDelayed skeletal maturationAbnormal femur morphologyShort noseOvoid vertebral bodiesSevere short statureShort palmFifth metacarpal with ulnar notchAbnormal epiphysis morphologyShort metacarpalSmall hand
Classification & Codes
MeSH Code
C535662Orphanet Code
ORPHA:969acromicric dysplasia
| MeSH | C535662 |
| Orphanet | ORPHA:969 |
| Treatments | 0 drug(s) |
| Symptoms on record | 22 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO