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Complete transverse basilar cleft associated with hemifacial microsomia.
Yurasakpong, Laphatrada; Suwannakhan, Athikhun; Iwanaga, Joe; Tubbs, R Shane; Chaiyamoon, Arada; Kruepunga, Nutmethee; Asuvapongpatana, Somluk; Sudsang, Thanwa.
Affiliation
  • Yurasakpong L; Department of Anatomy, Faculty of Science, Mahidol University, Bangkok, Thailand.
  • Suwannakhan A; In Silico and Clinical Anatomy Research Group (iSCAN), Bangkok, Thailand, Thailand.
  • Iwanaga J; Department of Anatomy, Faculty of Science, Mahidol University, Bangkok, Thailand.
  • Tubbs RS; In Silico and Clinical Anatomy Research Group (iSCAN), Bangkok, Thailand, Thailand.
  • Chaiyamoon A; Department of Neurosurgery, Tulane Center for Clinical Neurosciences, Tulane University School of Medicine, New Orleans, LA, USA.
  • Kruepunga N; Department of Neurology, Tulane Center for Clinical Neurosciences, Tulane University School of Medicine, New Orleans, LA, USA.
  • Asuvapongpatana S; Department of Oral and Maxillofacial Anatomy, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Sudsang T; Department of Structural and Cellular Biology, Tulane University School of Medicine, New Orleans, LA, USA.
Anat Cell Biol ; 57(3): 473-475, 2024 Sep 30.
Article in En | MEDLINE | ID: mdl-38449077
ABSTRACT
Transverse basilar cleft (TBC) is an extremely rare variation of the clivus or the basilar part of the occipital bone. In this report, a unilateral transverse basilar fissure was found at the clivus in a head computed tomography of an 18-year-old female patient diagnosed with hemifacial microsomia (HFM). Image analysis of this patient showed shortening of the ramus of the right mandible along with medial displacement of the right temporomandibular joint and hypoplastic right maxilla. In addition, observation of the clivus showed a cleft between the basioticum and basioccipital bones at the level of the pharyngeal tubercle on the right side. This cleft was identified as TBC. Clival variations, TBC included, attributed to HFM have never been reported. This report draws attention to the complex relationship between abnormal development of clivus and HFM syndrome, and sheds light on a possible genetic and molecular association between these two conditions.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Anat Cell Biol Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Anat Cell Biol Year: 2024 Document type: Article Affiliation country: Country of publication: