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mesomelic dysplasia, Kantaputra type

MeSH: C535547ORPHA: 1836

Contents

  1. 1. Overview
  2. 2. Available Treatments
  3. 3. Clinical Presentation
  4. 4. Classification & Codes

Overview

Mesomelic dysplasia Kantaputra type (MDK) is a rare skeletal disease characterized by symmetric shortening of the middle segments of limbs and short stature

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 mesomelic dysplasia, Kantaputra type, sourced from HPO and Orphanet clinical annotations.

Abnormal fibula morphologyMesomeliaAbnormality of the ankleShort statureDumbbell-shaped humerusTarsal synostosisCamptodactyly of fingerClinodactyly of the 5th fingerSynostosis of carpal bonesUlnar deviation of fingerAbnormal rib morphologyTalipesCubitus valgusVertebral segmentation defectAbnormal humerus morphology

Classification & Codes

MeSH Code

C535547

Orphanet Code

ORPHA:1836
mesomelic dysplasia, Kantaputra type
MeSHC535547
OrphanetORPHA:1836
Treatments0 drug(s)
Symptoms on record15 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO