Aminopterin/methotrexate embryofetopathy

Get in touch with RARE Concierge.

Contact RARE Concierge

Aminopterin/methotrexate embryofetopathy

Synonyms: Aminopterin embryopathy syndrome | Fetal aminopterin syndrome

A syndrome of developmental anomalies characterized by growth deficiency facial dysmorphism and skull limb and neural defects secondary to maternal exposure to aminopterin or methotrexate (MTX) during pregnancy.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version December 2023

Newly diagnosed with
Aminopterin/methotrexate embryofetopathy?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Clinical Trials

For a list of clinical trials in this disease area, please click here.