About Genee-Wiedemann Syndrome

Postaxial Acrofacial Dysostosis, also known as miller syndrome, is related to dysostosis and acrofacial dysostosis. An important gene associated with Postaxial Acrofacial Dysostosis is DHODH (Dihydroorotate Dehydrogenase (Quinone)), and among its related pathways/superpathways are Pyrimidine metabolism and PKMTs methylate histone lysines. The drugs Cimetidine and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include bone, eye and heart, and related phenotypes are microtia and micrognathia

Major Symptoms of Genee-Wiedemann Syndrome

Genee-Wiedemann syndrome is a rare autosomal recessive genetic disorder characterized by progressive joint hypermobility, joint stiffness, and decreased range of motion. It also often involves joint deformities, muscle weakness, and fatigue. Symptoms usually become apparent in the late teens or early twenties and can vary from person to person.

Suitable Lifestyle for People with Genee-Wiedemann Syndrome

An appropriate lifestyle approach for people with Gene-Wiedemann syndrome is to maintain a regular diet and engage in appropriate exercise. The syndrome often causes muscle weakness and atrophy, so patients may need to rely on muscle exercises to maintain muscle mass and strength. In the meantime, patients may need to follow their doctor's recommendations and receive appropriate treatment to help relieve symptoms and promote recovery.

Other Diseases

Wiedemann-Steiner Syndrome Stuve-Wiedemann Syndrome Beckwith-Wiedemann Syndrome KBG Syndrome Cat Eye Syndrome ICF Syndrome NDH Syndrome H Syndrome Dry Eye Syndrome FG Syndrome

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