Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Autosomal recessive brachyolmia

MONDO:0018662

Brachyolmia, recessive type is a form of brachyolmia, a group of rare genetic skeletal disorders, characterized by short-trunked short stature with platyspondyly and scoliosis. Corneal opacities and precocious calcification of the costal cartilage are rare syndromic components. Premature pubarche may occur.

Also known as: brachyolmia, Hobaek/Toledo type, brachyolmia, autosomal recessive

0 clinical trials for this condition and its sub-types, 0 tagged with Autosomal recessive brachyolmia itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of Autosomal recessive brachyolmia

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.