| Eponyms in category: Facial and orofacial |
| 62
main and alternative
entries found.
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| Ascher's syndrome |
| A combination of blepharochalasis, doublelip and, nontoxic goiter. |
| Ashley's syndrome |
| A syndrome of unusual facies, musculoskeletal anomalies, hip dislocation, scoliosis, vertical talus, and hand abnormalities. |
| Baelz' cheilitis |
| A rare disease with onset in childhood or early adolescence, characterized by enlargement, hardening, and finally eversion of the lip leading to exposure of the opening of the accessory salivary glands. |
| Baelz' syndrome (Baelz' cheilitis) |
| A rare disease with onset in childhood or early adolescence, characterized by enlargement, hardening, and finally eversion of the lip leading to exposure of the opening of the accessory salivary glands. |
| Balme's cough |
| Coughing due to nasopharyngeal obstruction when the patient lies down. |
| Berry's syndrome |
| Mandibulofacial dysostosis evident at birth. |
| Berry-Treacher Collins syndrome (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Brocq-Pautrier glossitis (Brocq-Pautrier syndrome) |
| Syndrome of a rhomboid and shiny lesion of area on the midline of base of tongue. |
| Brocq-Pautrier syndrome |
| Syndrome of a rhomboid and shiny lesion of area on the midline of base of tongue. |
| Brueghel’s syndrome (Meige's syndrome II) |
| A disabling spasm of the facial musculature consisting of primary blepharospasm followed by abnormal facial movement. |
| Burgio's pseudodiastrophic dwarfism |
| A syndrome characterised by short-limb dwarfim, brevicollis, clubfoot, joint contractures and dislocations, cleft palate, and characteristic facies. |
| Cervenka's syndrome |
| A syndrome caharacterised by facial abnormalities, joint deformity, and myopia. |
| Elschnig's syndrome |
| A rare malformation syndrome of palpebral fissures extending laterally. |
| Elschnig’s complex (Elschnig's syndrome) |
| A rare malformation syndrome of palpebral fissures extending laterally. |
| Franceschetti-Klein syndrome (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Franceschetti-Zwahlen syndrome (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Franceschetti-Zwahlen-Klein syndrome (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Franceschetti’s syndrome I (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Friedreich-Auerbach disease |
| Facial hemihypertrophy involving the eyelids, cheeks, lips, facial bones, tongue, ears, and tonsils. |
| Friedreich’s disease (Friedreich-Auerbach disease) |
| Facial hemihypertrophy involving the eyelids, cheeks, lips, facial bones, tongue, ears, and tonsils. |
| Fuchs’ syndrome III (Ascher's syndrome) |
| A combination of blepharochalasis, doublelip and, nontoxic goiter. |
| Gorlin's syndrome (Papillon-Léage and Psaume syndrome) |
| A congenital syndrome characterised by orofacial and digital defects. |
| Gorlin-Psaume syndrome (Papillon-Léage and Psaume syndrome) |
| A congenital syndrome characterised by orofacial and digital defects. |
| Greig's ocular hypertelorism syndrome (Greig's syndrome II) |
| Hereditary/familial ocular hypertelorism. Pesents as abnormal increase in distance between the eyes due to development arrest of the greater wings of the sphenoid bone. |
| Greig's syndrome II |
| Hereditary/familial ocular hypertelorism. Pesents as abnormal increase in distance between the eyes due to development arrest of the greater wings of the sphenoid bone. |
| Greig's’ disease (Greig's syndrome II) |
| Hereditary/familial ocular hypertelorism. Pesents as abnormal increase in distance between the eyes due to development arrest of the greater wings of the sphenoid bone. |
| Hunter's glossitis (William Hunter) |
| Ucerous glossitis in pernicious anaemia. |
| Klein-Waardenburg syndrome |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| Klein’s syndrome (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| Laehr-Henneberg hard palate |
| Tickling of the hard palate results in contraction of the orbicularis oris and lowering of the upper lip in pseudo-bulbar palsy.
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| Laffer-Ascher syndrome (Ascher's syndrome) |
| A combination of blepharochalasis, doublelip and, nontoxic goiter. |
| Lingua Brocq-Pautrier (Brocq-Pautrier syndrome) |
| Syndrome of a rhomboid and shiny lesion of area on the midline of base of tongue. |
| Maier's sinus |
| A depression of the internal surface of the lacrimal sac which receive the lacrimal canaliculi. |
| Meige's syndrome II |
| A disabling spasm of the facial musculature consisting of primary blepharospasm followed by abnormal facial movement. |
| Mende's syndrome II (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| Miescher's cheilitis |
| Granulomatous cheilitis as a monosymptomatic form of the Melkersson-Rosenthal syndrome. |
| Miescher’s syndrome (Miescher's cheilitis) |
| Granulomatous cheilitis as a monosymptomatic form of the Melkersson-Rosenthal syndrome. |
| Möller's glossitis (Hunter's glossitis (William Hunter)) |
| Ucerous glossitis in pernicious anaemia. |
| Möller's glossitis (William Hunter) |
| Superficial excorcitation of the tongue, principally of its tip and edges. |
| Möller-Hunter glossitis (Hunter's glossitis (William Hunter)) |
| Ucerous glossitis in pernicious anaemia. |
| Möller-Hunter syndrome (Hunter's glossitis (William Hunter)) |
| Ucerous glossitis in pernicious anaemia. |
| Papillon-Léage and Psaume syndrome |
| A congenital syndrome characterised by orofacial and digital defects. |
| Parry-Romberg syndrome |
| A rare disorder characterized by progressive atrophy of some or all tissues on one side of the face, occasionally extending to other parts of the body. |
| 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). |
| Psaume’s syndrome (Papillon-Léage and Psaume syndrome) |
| A congenital syndrome characterised by orofacial and digital defects. |
| Puente's disease (Baelz' cheilitis) |
| A rare disease with onset in childhood or early adolescence, characterized by enlargement, hardening, and finally eversion of the lip leading to exposure of the opening of the accessory salivary glands. |
| Robin's anomalad (Robin's syndrome) |
| A very rare congenital malformation syndrome characterized by unusual smallness of the jaw combined with cleft palate, downward displacement of the tongue, and an absent gag reflex. |
| Robin's syndrome |
| A very rare congenital malformation syndrome characterized by unusual smallness of the jaw combined with cleft palate, downward displacement of the tongue, and an absent gag reflex. |
| Robin’s sequence (Robin's syndrome) |
| A very rare congenital malformation syndrome characterized by unusual smallness of the jaw combined with cleft palate, downward displacement of the tongue, and an absent gag reflex. |
| Romberg’s disease (Parry-Romberg syndrome) |
| A rare disorder characterized by progressive atrophy of some or all tissues on one side of the face, occasionally extending to other parts of the body. |
| Thomson complex (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Treacher Collins syndrome (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Treacher Collins-Franceschetti syndrome (Berry's syndrome) |
| Mandibulofacial dysostosis evident at birth. |
| Van der Hoeve's symptom |
| Enlargement of Mariotte’s spot in inflammation of the sinuses of the nose.
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| Van der Hoeve-Halbertsma-Gualdi syndrome (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| van der Hoeve-Halbertsma-Waardenburg syndrome (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| van der Hoeve-Waardenburg-Klein syndrome (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| Villaret's syndrome |
| A syndrome of ipsilateral paralysis of the ninth, tenth, eleventh, twelfth, and sometimes the seventh cranial nerves and the cervical sympathetic fibers. |
| Vogt’s syndrome (Cécile Vogt) (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
| Volkmann's cheilitis (Baelz' cheilitis) |
| A rare disease with onset in childhood or early adolescence, characterized by enlargement, hardening, and finally eversion of the lip leading to exposure of the opening of the accessory salivary glands. |
| Waardenburg's syndrome II (Klein-Waardenburg syndrome) |
| A hereditary congenital defect involving pigmentation, lateral displacement of the medial canthi and lacrimal points, and deafness. |
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