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

C535662

Orphanet Code

ORPHA:969
acromicric dysplasia
MeSHC535662
OrphanetORPHA:969
Treatments0 drug(s)
Symptoms on record22 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO