Molar tooth sign of the midbrain-hindbrain junction: Occurrence in multiple distinct syndromes

被引:174
作者
Gleeson, JG
Keeler, LC
Parisi, MA
Marsh, SE
Chance, PF
Glass, IA
Graham, JM
Maria, BL
Barkovich, AJ
Dobyns, WB
机构
[1] Univ Calif San Diego, Dept Neurosci, Div Pediat Neurol, La Jolla, CA 92093 USA
[2] Univ Washington, Childrens Hosp & Reg Med Ctr, Div Genet & Dev, Washington, DC USA
[3] Univ Calif Los Angeles, Sch Med, Cedars Sinai Med Ctr, Ahmanson Dept Pediat,Med Genet Birth Defects Ctr, Los Angeles, CA USA
[4] Univ Missouri, Dept Child Hlth, Columbia, MO 65211 USA
[5] Univ Calif San Francisco, Dept Radiol, San Francisco, CA 94143 USA
[6] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[7] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[8] Univ Calif San Francisco, Dept Neurosurg, San Francisco, CA 94143 USA
[9] Univ Chicago, Dept Human Genet, Chicago, IL 60637 USA
关键词
Joubert; molar tooth; Varadi-Papp; OFD-VI; COACH; Senior-Loken; Dekaban-Arima; cerebellar vermis; hypotonia; ataxia; oculomotor apraxia; kidney cysts; nephronophthisis; hepatic fibrosis; Leber congenital amaurosis; polymicrogyria; coloboma; encephalocele;
D O I
10.1002/ajmg.a.20437
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Molar Tooth Sign (MTS) is defined by an abnormally deep interpeduncular fossa; elongated, thick, and mal-oriented superior cerebellar peduncles; and absent or hypoplastic cerebellar vermis that together give the appearance of a "molar tooth" on axial brain MRI through the junction of the midbrain and hindbrain (isthmus region). It was first described in Joubert syndrome (JS) where it is present in the vast majority of patients with this diagnosis. We previously showed that the MTS is a component of several other syndromes, including Dekaban-Arima (DAS), Senior-Loken, and COACH (cerebellar vermis hypoplasia (CVH), oligophrenia, ataxia, coloboma, and hepatic fibrosis). Here we present evidence that the MTS is seen together with polymicrogyria, Varadi-Papp syndrome (Orofaciodigital VI (OFD VI)), and a new syndrome with encephalocele and cortical renal cysts. We also present a new patient with COACH syndrome plus the MTS. We propose that the MTS is found in multiple distinct clinical syndromes that may share common developmental mechanisms. Proper classification of patients with these variants of the MTS will be essential for localization and identification of mutant genes. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:125 / 134
页数:10
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