Femoral facial syndrome

Verloes Van Maldergem Marneffe Syndrome. A rare genetic disorder characterized by underdeveloped femur, short nose and cleft palate. From Wikipedia, the free encyclopedia. Report of three cases. This page was last edited on 15 March , at This means that Femoral facial syndrome, or a subtype of Femoral facial syndrome, affects less than , people in the US population. Schaefer Stein Oshman Syndrome.
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Proximal Femoral Focal Deficiency Differential Diagnoses

A case of femoral-facial syndrome in a patient with autism spectrum disorders. Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2, National Institutes of Health. These resources provide more information about this condition or associated symptoms. Abnormally shaped ears Auricular malformation Deformed ears Malformed ears Simple ears [ more ]. Jung Wolff Back Stahl Syndrome.
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Femoral–facial syndrome with malformations in the central nervous system - ScienceDirect

Dianzani Autoimmune Lymphoproliferative Syndrome. Jung Wolff Back Stahl Syndrome. We are determined to keep this website freely accessible. Cyprus Facial Neuromusculoskeletal Syndrome. Muller Barth Menger Syndrome. Say Field Coldwell syndrome. Or filter your current search.
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Intellectual development was normal in most cases. If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. There were upper limb contractures, and the legs consisted primarily of tibia and fibula with bilateral clubfeet. Value of magnetic resonance imaging in early assessment of proximal femoral focal deficiency PFFD. Some cases have been reported in association with diabetes in the mother during pregnancy. Femoral facial syndrome with bilateral agenesis of femora and preaxial polydactyly of the feet in a Chinese stillborn. A case of femoral-facial syndrome in a patient with autism spectrum disorders.
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