| Eponyms in category: Craniofacial |
| 26
main and alternative
entries found.
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| André's syndrome |
| A syndrome of peculiar facies and osseous defect.
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| Apert's syndactyly (Apert's syndrome) |
| A complex of craniofacial abnormalities caused by premature craniosynostosis, usually of the coronal suture, leading to turribrachycephaly, associated with syndactyly and polydactyly. |
| Apert's syndrome |
| A complex of craniofacial abnormalities caused by premature craniosynostosis, usually of the coronal suture, leading to turribrachycephaly, associated with syndactyly and polydactyly. |
| Apert-Crouzon syndrome |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Cervenka’s syndrome (Pepper's syndrome) |
| An inherited disorder characterized by craniofacial anomalies, skeletal abnormalities, obesity, mental retardation, and myotonia; without short stature or hypogonadism. |
| Cohen's syndrome (Pepper's syndrome) |
| An inherited disorder characterized by craniofacial anomalies, skeletal abnormalities, obesity, mental retardation, and myotonia; without short stature or hypogonadism. |
| Crouzon's syndrome |
| Craniostosis with widening of the skull and high forehead, ocular hypertelorism, exophthalmos, beaked nose, and hypoplasia of the maxilla. |
| Crouzon-Apert disease (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Crouzon’s syndrome (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Dysostosis craniofacialis Crouzon (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Emery-Nelson syndrome |
| Disturbance characterized by the trias of short stature, deformities of hands and feet, and unusual facies. |
| Escobar's syndrome |
| A rare syndrome of short stature, craniofacial anomalies, joint contractures, vertebral fusion anomalies, rocker-bottom feet, and pterygia of the neck, antecubital, digital, poplietal, and intercrural areas. |
| Fairbank-Keats syndrome |
| A rare form of bone dysplasia characterised by distinctive bone lesions, disproportionate dwarfism, and severe craniofacial defect. |
| Hootnick-Holmes syndrome |
| A familial syndrome of polysyndactyly, craniofacial anomalies, mental retardation, etc. |
| Melnick-Fraser syndrome I |
| A very rare genetic disorder characterised by distinctive malformations of the head and facial area, with skin lesions and abnormalities of the eyes. |
| Melnick-Needles syndrome |
| A very rare syndrome of generalised bone dysplasia with stunted stature, and multiple craniofacial abnormalities. |
| Neuhäuser's MMR syndrome |
| Inheritable malformation-retardation syndrome with enlarged corneas, other eye anomalies, craniofacial dysmorphy and cerebral attacks. |
| Pepper's syndrome |
| An inherited disorder characterized by craniofacial anomalies, skeletal abnormalities, obesity, mental retardation, and myotonia; without short stature or hypogonadism. |
| Potter's ear |
| Characteristic low set flat ears deficient in cartilage. A feature of Potter's facies. |
| Potter's facies |
| Characteristic facies seen in severe renal malformations (Potters' disease). |
| Pseudo-Crouzon’s syndrome (Franceschetti’s) (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Taybi's syndrome (André's syndrome) |
| A syndrome of peculiar facies and osseous defect.
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| Virchow’s oxycephaly (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Vogt 's syndrome (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Vogt’s cephalosyndactyly (Apert-Crouzon syndrome) |
| A rare form of Carpenter's syndrome (acrocephalopoysyndactyly) combining features of the Apert syndrome with those of the Crouzon syndrome. |
| Weisenburg-Sicard-Robineau syndrome |
| A disturbance characterized by paroxysms of sharp shooting pain starting in the tonsillar region. |
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