Fraser Syndrome

Overview

Rare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies of bone, ear, lung, and nose are common. Mutations on FRAS1 and FREM2 are associated with the syndrome.

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Fraser Syndrome

Topic type

Condition

Category

Ophthalmology

MeSH classification

C05.116.099.370.894.819.428|C05.660.585.800.428|C05.660.906.819.428|C11.250.390|C12.050.351.875.397|C12.200.706.410|C12.800.410|C16.131.077.371|C16.131.384.442|C16.131.621.585.800.428|C16.131.621.906.819.428|C16.131.939.410

Preparing for an appointment about Fraser Syndrome

If you are speaking with a healthcare professional about Fraser Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

Finding care related to Fraser Syndrome

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