Literature DB >> 7266779

Joubert syndrome: clinical and polygraphic observations in a further case.

E Boltshauser, M Herdan, G Dumermuth, W Isler.   

Abstract

To our knowledge, only 10 cases of Joubert syndrome have been published so far. In this paper, we describe the clinical, radiological (computerized tomography) and polygraphic findings in an additional patient. The female presented here is the product of consanguineous parents and a sibling of a previously reported infant. In addition to the well-known episodic tachypnea in an awake state, representing the clinical hallmark of this syndrome, this child also had bouts of tachypnea while asleep. Interestingly enough, these were confined only to non-REM sleep.

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Year:  1981        PMID: 7266779     DOI: 10.1055/s-2008-1059650

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  15 in total

Review 1.  Joubert Syndrome and related disorders.

Authors:  Francesco Brancati; Bruno Dallapiccola; Enza Maria Valente
Journal:  Orphanet J Rare Dis       Date:  2010-07-08       Impact factor: 4.123

2.  When is biopsy-proven TIN not simply TIN? Answers.

Authors:  Nicholas Ware; Neil J Sebire; W K Chong; Rajesh Krishnan; Stephen D Marks
Journal:  Pediatr Nephrol       Date:  2016-10-07       Impact factor: 3.714

3.  Joubert syndrome in a neonate: case report with literature review.

Authors:  Haifa A Bin Dahman; Abdul-Hakeem M Bin Mubaireek; Zain H Alhaddad
Journal:  Sudan J Paediatr       Date:  2016

Review 4.  Healthcare recommendations for Joubert syndrome.

Authors:  Ruxandra Bachmann-Gagescu; Jennifer C Dempsey; Sara Bulgheroni; Maida L Chen; Stefano D'Arrigo; Ian A Glass; Theo Heller; Elise Héon; Friedhelm Hildebrandt; Nirmal Joshi; Dana Knutzen; Hester Y Kroes; Stephen H Mack; Sara Nuovo; Melissa A Parisi; Joseph Snow; Angela C Summers; Jordan M Symons; Wadih M Zein; Eugen Boltshauser; John A Sayer; Meral Gunay-Aygun; Enza Maria Valente; Dan Doherty
Journal:  Am J Med Genet A       Date:  2019-11-11       Impact factor: 2.802

5.  [A rare form of optical, choroidal and retinal dysplasia combined with an occipital encephalocele].

Authors:  U Mayer; M Klinger; H D Rott
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1982       Impact factor: 3.117

6.  Joubert-Boltshauser syndrome with polydactyly in siblings.

Authors:  J Egger; M H Bellman; E M Ross; M Baraitser
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-08       Impact factor: 10.154

Review 7.  MRI of the fetal posterior fossa.

Authors:  Catherine Adamsbaum; Marie Laure Moutard; Christine André; Valérie Merzoug; Solène Ferey; Marie Pierre Quéré; Fanny Lewin; Catherine Fallet-Bianco
Journal:  Pediatr Radiol       Date:  2004-11-23

8.  Analysis and classification of cerebellar malformations.

Authors:  Sandeep Patel; A James Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

9.  Joubert syndrome: a clinico-radiological study.

Authors:  B Kendall; D Kingsley; S R Lambert; D Taylor; P Finn
Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

10.  Congenital muscular dystrophy and cerebellar vermis agenesis in two brothers.

Authors:  O Arancio; L G Bongiovanni; G Bonadonna; G Tomelleri; D De Grandis
Journal:  Ital J Neurol Sci       Date:  1988-10
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