| Clinical Study of Symptoms and Various Anomalies of Patients with Joubert Syndrome |
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Hang Bo Jeong, Se Hee Hwang, Ki Joong Kim, Yong Seung Hwang, Seung Cheol Kim, In-One Kim |
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Department of Pediatrics, College of Medicine, Seoul National University, Seoul, Korea |
| Joubert증후군의 증상 및 형태학적 병변에 대한 임상적 고찰 |
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정항보, 황세희, 김기중, 황용승, 김승철, 김인원 |
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서울대학교 의과대학 소아과학교실 |
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| Abstract |
Purpose
: Joubert syndrome is known tobean autosomal recessive disorder characterized
by cerebellar vermian dysgenesis with many symptoms and variety of other
malformations. We studied the relevant symptoms and various malformations of seven
patients diagnosed as Joubert syndrome at our institution.
Methods
: Seven children with cerebellarvermian dysgenesis consistent with Joubert
syndrome were included in ourstudy. Each child was diagnosed at the Seoul National
University Children's Hospital from Feb. 1991 to Feb. 1995. We studied the frequency of eachsymptom ofJoubert syndrome and the associated malformations of the selected cases.
Results
: All seven patients had no family members affected. Also their parental
consanguinity were not found. Sex ratio was 1.3:1(4 males and 3 females) showing no
significant sex difference. Ages at diagnosis were less than one year old. Six patients in our study had developmental delay,which was the most frequent symptom. Four patients had ataxia; four patients had hypotonia; three patients had abnormal ocular movements such as nystagmus or saccadic palsy; only one patient had episodic tachypnea in neonatalperiod;and in one case there were tongue protrusion and seizure,
respectively. In two cases there were occipital meningoceles, agenesis of corpus
callosum, and cleft palates, respectively. In one case there were cystic renal disorder, neuronal heterotopia, absence of septum pellucidum, and polydactyly, respectively. None had retinal dystrophy or chorioretinal coloboma.
Conclusion
: The cardinal symptoms of Joubert syndrome are unexplainable episodic tachypnea alternating with apnea during neonatal period, abnormal ocular movement
such as nystagmus or saccadic palsy, ataxia, hypotonia, and developmental delay. The
presence of such symptoms should alert the clinician to apply appropriate test such as neuroradiologic study including brain MRI etc. Some of the inconstantly associated
features of Joubert syndrome include congenital retinal dystrophy, chorioretinal coloboma, and cystic kidney disease. The patients should be examined routinely with electroretinogram, fundoscopy, and kidney ultrasonogram for early detection or exclusion of the associated anomalies. We stress the importance of genetic counselling for the families of Joubert syndrome as well as that of the prompt supportive therapy for the patient. |
| Key Words:
Joubert syndrome, , Cerebellar vermis agenesis, Retinal dystrophy, Chorioretial coloboma, Neonatal tachypnea, Ataxia, Development delay |
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