^
Fact-checked
х

All iLive content is medically reviewed or fact checked to ensure as much factual accuracy as possible.

We have strict sourcing guidelines and only link to reputable media sites, academic research institutions and, whenever possible, medically peer reviewed studies. Note that the numbers in parentheses ([1], [2], etc.) are clickable links to these studies.

If you feel that any of our content is inaccurate, out-of-date, or otherwise questionable, please select it and press Ctrl + Enter.

Brachymetacarpy: causes, symptoms, diagnosis, treatment

Medical expert of the article

Pediatric orthopedist, pediatrician, traumatologist, surgeon
, medical expert
Last reviewed: 04.07.2025

Brachymetacarpia is a congenital defect caused by a violation of the differentiation of the bone-articular apparatus of the hand and expressed in the shortening of the metacarpal bones.

ICD-10 code

Q74.0 Brachymetacarpy.

Symptoms of Brachymetacarpia

Clinically, in children over 8 years of age, growth retardation of the metacarpal bones (usually III, IV, V) is observed due to early closure of the metaepiphyseal growth zones, determined by radiography. The functions of the hand are not affected, and the main complaint of patients is the aesthetic defect of the recession of the heads of the deformed metacarpal bones, which determines the shortening of the corresponding ray as a whole.

Treatment of brachymetacarpy

There are two treatment options. First, the defect can be corrected by lengthening the affected metacarpal bones using a distraction device. The second treatment option is one-stage bone grafting of the shortened metacarpal bones using a spongy-cortical bone graft from the iliac wing.

trusted-source[ 1 ]

What do need to examine?


The iLive portal does not provide medical advice, diagnosis or treatment.
The information published on the portal is for reference only and should not be used without consulting a specialist.
Carefully read the rules and policies of the site. You can also contact us!

Copyright © 2011 - 2025 iLive. All rights reserved.