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• Ethylin Wang Jabs
  ...genetic causes of [[Apert syndrome]], [[Crouzon syndrome]], and [[Pfeiffer syndrome]], among others. * [[Apert syndrome]]
  2 KB (193 words) - 19:54, 11 February 2024
• Pashayan syndrome
  == Pashayan Syndrome == ...ability]], [[growth retardation]], and [[craniofacial abnormalities]]. The syndrome was first described by Dr. Harry Pashayan in 1979.
  2 KB (235 words) - 11:50, 10 February 2024
• Craniofacial abnormalities
  ...gnancy. Some conditions, such as [[Treacher Collins Syndrome]] and [[Apert Syndrome]], are caused by specific genetic mutations.
  2 KB (292 words) - 07:09, 13 February 2024
• Craniofacial dysostosis
  * [[Crouzon syndrome]] * [[Apert syndrome]]
  1 KB (168 words) - 06:42, 11 February 2024
• Raine syndrome
  '''Raine Syndrome''' ...osteosclerosis, craniofacial dysmorphism, and cerebral calcification. The syndrome is named after the Australian pediatrician, Dr. Michael Raine, who first de
  2 KB (245 words) - 04:43, 9 February 2024
• Daentl Townsend Siegel syndrome
  '''Daentl Townsend Siegel syndrome''' (pronounced: Day-ntl Town-send See-gel syndrome) is a rare genetic disorder characterized by specific physical abnormalitie The syndrome is named after the three doctors, Dr. Daentl, Dr. Townsend, and Dr. Siegel,
  2 KB (235 words) - 19:41, 12 February 2024
• Treacher collins syndrome
  '''Treacher Collins Syndrome''' ...is a rare genetic disorder characterized by craniofacial deformities. The syndrome is named after Edward Treacher Collins, the British ophthalmologist who fir
  2 KB (260 words) - 04:03, 12 February 2024
• Treacher Collins syndrome
  ...is a rare genetic disorder characterized by craniofacial deformities. The syndrome is named after Edward Treacher Collins, the British ophthalmologist who fir The term "Treacher Collins syndrome" is derived from the name of its identifier, Edward Treacher Collins. The t
  2 KB (249 words) - 04:28, 12 February 2024
• Fetal trimethadione syndrome
  '''Fetal Trimethadione Syndrome''' '''Fetal Trimethadione Syndrome''' (pronunciation: fee-tal try-meth-oh-dye-on sin-drome) is a rare [[congen
  2 KB (204 words) - 04:35, 12 February 2024
• Craniofacial abnormality
  * '''[[Treacher Collins syndrome]]''': This is a genetic disorder characterized by deformities of the ears,
  2 KB (323 words) - 14:49, 11 February 2024
• Zechi-Ceide syndrome
  '''Zechi-Ceide Syndrome''' '''Zechi-Ceide Syndrome''' (pronounced: Zeh-kee Say-dee Syndrome) is a rare genetic disorder characterized by specific facial features, abno
  2 KB (242 words) - 05:54, 11 February 2024
• Rudiger syndrome
  == Rudiger Syndrome == '''Rudiger Syndrome''' (pronounced: roo-dih-ger sin-drome) is a rare genetic disorder character
  2 KB (301 words) - 23:17, 9 February 2024
• Glossoptosis
  ...ofacial abnormalities such as [[Treacher Collins syndrome]] and [[Stickler syndrome]]. * [[Treacher Collins syndrome]]
  2 KB (233 words) - 00:01, 7 February 2024
• Zadik Barak Levin syndrome
  '''Zadik Barak Levin Syndrome''' '''Zadik Barak Levin Syndrome''' (''Za-dik Ba-rak Le-vin Syn-drome'') is a rare genetic disorder characte
  2 KB (257 words) - 06:24, 12 February 2024
• 3C syndrome
  == 3C Syndrome == '''3C Syndrome''' (pronounced: three-see syndrome), also known as '''Craniocerebellocardiac Dysplasia''' (pronounced: kray-ne
  2 KB (309 words) - 23:15, 3 February 2024
• Kapur Toriello syndrome
  '''Kapur Toriello syndrome''' is a rare genetic disorder characterized by a variety of physical abnorm Kapur Toriello syndrome is pronounced as "Kah-pur Tor-ee-ello Syn-drome".
  2 KB (241 words) - 02:59, 12 February 2024
• Dolichocephaly
  ...d with certain genetic syndromes, such as [[Sotos syndrome]] and [[Crouzon syndrome]]. * [[Sotos syndrome]]
  1 KB (199 words) - 04:39, 7 February 2024
• Fetal hydantoin syndrome
  '''Fetal Hydantoin Syndrome''' '''Fetal hydantoin syndrome''' (pronunciation: fee-tal hy-dan-toin sin-drome) is a disorder that occurs
  2 KB (235 words) - 02:53, 12 February 2024
• Goldenhar Syndrome
  == Goldenhar Syndrome == ...rder characterized by abnormal development of the eye, ear, and spine. The syndrome was first described by the Swiss ophthalmologist Maurice Goldenhar in 1952.
  2 KB (262 words) - 22:57, 14 February 2024
• Roberts syndrome
  == Roberts syndrome == ...rowth retardation, craniofacial abnormalities, and limb malformations. The syndrome is named after [[John Bingham Roberts]], a prominent American surgeon who f
  2 KB (306 words) - 23:30, 9 February 2024

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