Acinar dysplasia

MONDO:0600016

A lethal, developmental lung malformation resulting in neonatal respiratory insufficiency. It is characterized by pulmonary hypoplasia and arrest in the pseudoglandular stage of development, resulting in the absence of functional gas exchange. It can be caused by mutations in FGF10, FGFR2 or TBX4.

Also known as: AcDys

0 clinical trials for this condition and its sub-types, 0 tagged with Acinar dysplasia itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Respiratory system disorder (10848)

Sub-types of Acinar dysplasia

Acinar dysplasia caused by mutation in FGF10 0 trials
Acinar dysplasia caused by mutation in FGFR2 0 trials
Acinar dysplasia caused by mutation in TBX4 0 trials

Including sub-types (0) Tagged with Acinar dysplasia (0)

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