Mesomelic Dysplasia, Kantaputra Type


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

Clinical Features

Top most frequent phenotypes and symptoms related to Mesomelic Dysplasia, Kantaputra Type

  • Short stature
  • Flexion contracture
  • Abnormality of the skeletal system
  • Talipes equinovarus
  • Clinodactyly of the 5th finger
  • Skeletal dysplasia
  • Camptodactyly of finger
  • Talipes
  • Limb undergrowth
  • Abnormality of the ribs

And another 16 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Alternative names

Mesomelic Dysplasia, Kantaputra Type Is also known as kantaputra mesomelic dysplasia, mesomelic dysplasia, thai type, mdk, mesomelic dysplasia with ankle, carpal, and tarsal synostosis.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Sources and references

You can check the following sources for additional information.

OMIM ORPHANET Rare Disease Symptoms Checker

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