TY - JOUR
T1 - Cerebello-oculo-renal syndromes including Arima, Senior-Loken and COACH syndromes
T2 - More than just variants of joubert syndrome
AU - Satran, Daniel
AU - Pierpont, Mary Ella M.
AU - Dobyns, William B.
PY - 1999/10/29
Y1 - 1999/10/29
N2 - Cerebellar vermis hypoplasia (CVH) is part of many different malformation syndromes, especially Joubert syndrome. However, the nosology of these disorders remains uncertain. We reviewed reports of 100 children with cerebellar vermis hypoplasia, and ocular or renal involvement. Although the status of the upper brainstem was not adequately documented in most of these patients, some had hypoplasia and dysplasia of the ponto-mesencephalic isthmus and the superior portion of the cerebellar vermis, which results in a 'molar tooth' sign on MRI scan. Several distinct syndromes were apparent among this group. We conclude that (a) hypoplasia of the cerebellar vermis, especially the anterior vermis, is often associated with a complex brainstem malformation; (b) the latter comprises a 'molar tooth' brainstem and vermis hypoplasia-dysplasia malformation complex; (c) this complex may include the Dandy-Walker malformation, occipital cephalocele, and some abnormalities of the cerebrum as evidenced by frequent mental retardation; and (d) the 'molar tooth' sign or malformation is causally heterogeneous as it occurs in several distinct malformation syndromes including Joubert syndrome, Arima syndrome, Senior-Loken syndrome, COACH syndrome, and probably familial juvenile nephronophthisis.
AB - Cerebellar vermis hypoplasia (CVH) is part of many different malformation syndromes, especially Joubert syndrome. However, the nosology of these disorders remains uncertain. We reviewed reports of 100 children with cerebellar vermis hypoplasia, and ocular or renal involvement. Although the status of the upper brainstem was not adequately documented in most of these patients, some had hypoplasia and dysplasia of the ponto-mesencephalic isthmus and the superior portion of the cerebellar vermis, which results in a 'molar tooth' sign on MRI scan. Several distinct syndromes were apparent among this group. We conclude that (a) hypoplasia of the cerebellar vermis, especially the anterior vermis, is often associated with a complex brainstem malformation; (b) the latter comprises a 'molar tooth' brainstem and vermis hypoplasia-dysplasia malformation complex; (c) this complex may include the Dandy-Walker malformation, occipital cephalocele, and some abnormalities of the cerebrum as evidenced by frequent mental retardation; and (d) the 'molar tooth' sign or malformation is causally heterogeneous as it occurs in several distinct malformation syndromes including Joubert syndrome, Arima syndrome, Senior-Loken syndrome, COACH syndrome, and probably familial juvenile nephronophthisis.
KW - Arima syndrome
KW - COACH syndrome
KW - Congenital oculomotor apraxia
KW - Cystic dysplastic kidneys
KW - Joubert syndrome
KW - Juvenile nephronophthisis
KW - Leber congenital amaurosis
KW - Molar tooth malformation
KW - Retinopathy
KW - Senior-Loken syndrome
KW - Vermis
KW - Vermis hypoplasia
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U2 - 10.1002/(SICI)1096-8628(19991029)86:5<459::AID-AJMG12>3.0.CO;2-C
DO - 10.1002/(SICI)1096-8628(19991029)86:5<459::AID-AJMG12>3.0.CO;2-C
M3 - Article
C2 - 10508989
AN - SCOPUS:0033615477
SN - 0148-7299
VL - 86
SP - 459
EP - 469
JO - American Journal of Medical Genetics
JF - American Journal of Medical Genetics
IS - 5
ER -