Condition
Orofaciodigital Syndromes
Orthopaedics
Overview
Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait.
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 Orofaciodigital Syndromes
- Topic type
- Condition
- Category
- Orthopaedics
- MeSH classification
- C05.116.099.370.652|C05.660.207.700|C16.131.077.676|C16.131.260.830.670|C16.131.621.207.700|C16.320.180.830.670|C16.320.714
Preparing for an appointment about Orofaciodigital Syndromes
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- 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.
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.