Literature DB >> 31015250

Joubert syndrome with multiple pituitary hormone deficiency.

Nese Akcan1, Firdevs Bas2, Sukran Poyrazoglu2, Ruveyde Bundak3.   

Abstract

Joubert syndrome (JS) and JS-related disorders are a group of developmental delay, multiple congenital anomalies and complex midbrain-hindbrain malformations. A few cases of JS with multiple pituitary hormone deficiency (MPHD) have been reported in literature. Here, we presented an unusual presentation of JS in a newborn with MPHD. This case is intended to draw attention to the rare association of JS and MDPH by increasing the awareness of this syndrome. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  neuroendocrinology; neuroimaging; pituitary disorders

Mesh:

Substances:

Year:  2019        PMID: 31015250      PMCID: PMC6505975          DOI: 10.1136/bcr-2018-229016

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  11 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

Review 2.  Clinical and molecular features of Joubert syndrome and related disorders.

Authors:  Melissa A Parisi
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

3.  Mutations in KIAA0753 cause Joubert syndrome associated with growth hormone deficiency.

Authors:  Joshi Stephen; Thierry Vilboux; Luhe Mian; Chulaluck Kuptanon; Courtney M Sinclair; Deniz Yildirimli; Dawn M Maynard; Joy Bryant; Roxanne Fischer; Meghana Vemulapalli; James C Mullikin; Marjan Huizing; William A Gahl; May Christine V Malicdan; Meral Gunay-Aygun
Journal:  Hum Genet       Date:  2017-02-20       Impact factor: 4.132

4.  AN UNUSUAL PRESENTATION OF JOUBERT SYNDROME AND RELATED DISORDERS IN A NEWBORN: PANHYPOPITUITARISM.

Authors:  S Erol; N Demirel; A Y Bas; B Ozcan; I H Celik; D Ulubas Isik
Journal:  Genet Couns       Date:  2016

5.  Absent pituitary gland and hypoplasia of the cerebellar vermis associated with partial ophthalmoplegia and postaxial polydactyly: a variant of orofaciodigital syndrome VI or a new syndrome?

Authors:  L I Al-Gazali; L Sztriha; J Punnose; W Shather; M Nork
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

6.  The 'molar tooth sign' in Joubert syndrome.

Authors:  Imaad ur Rehman; Zablon Bett; Yousuf Husen; Ali Syed Muhammad Akhtar; Faisal Aziz Khan
Journal:  J Pak Med Assoc       Date:  2009-12       Impact factor: 0.781

7.  CELSR2, encoding a planar cell polarity protein, is a putative gene in Joubert syndrome with cortical heterotopia, microophthalmia, and growth hormone deficiency.

Authors:  Thierry Vilboux; May Christine V Malicdan; Joseph C Roney; Andrew R Cullinane; Joshi Stephen; Deniz Yildirimli; Joy Bryant; Roxanne Fischer; Meghana Vemulapalli; James C Mullikin; Peter J Steinbach; William A Gahl; Meral Gunay-Aygun
Journal:  Am J Med Genet A       Date:  2017-01-04       Impact factor: 2.802

Review 8.  Joubert syndrome: congenital cerebellar ataxia with the molar tooth.

Authors:  Marta Romani; Alessia Micalizzi; Enza Maria Valente
Journal:  Lancet Neurol       Date:  2013-07-17       Impact factor: 44.182

9.  Mutational analysis of the RPGRIP1L gene in patients with Joubert syndrome and nephronophthisis.

Authors:  M T F Wolf; S Saunier; J F O'Toole; N Wanner; T Groshong; M Attanasio; R Salomon; T Stallmach; J A Sayer; R Waldherr; M Griebel; J Oh; T J Neuhaus; U Josefiak; C Antignac; E A Otto; F Hildebrandt
Journal:  Kidney Int       Date:  2007-10-24       Impact factor: 10.612

10.  The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.

Authors:  Marion Delous; Lekbir Baala; Rémi Salomon; Christine Laclef; Jeanette Vierkotten; Kàlmàn Tory; Christelle Golzio; Tiphanie Lacoste; Laurianne Besse; Catherine Ozilou; Imane Moutkine; Nathan E Hellman; Isabelle Anselme; Flora Silbermann; Christine Vesque; Christoph Gerhardt; Eleanor Rattenberry; Matthias T F Wolf; Marie Claire Gubler; Jéléna Martinovic; Féréchté Encha-Razavi; Nathalie Boddaert; Marie Gonzales; Marie Alice Macher; Hubert Nivet; Gérard Champion; Jean Pierre Berthélémé; Patrick Niaudet; Fiona McDonald; Friedhelm Hildebrandt; Colin A Johnson; Michel Vekemans; Corinne Antignac; Ulrich Rüther; Sylvie Schneider-Maunoury; Tania Attié-Bitach; Sophie Saunier
Journal:  Nat Genet       Date:  2007-06-10       Impact factor: 38.330

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  1 in total

Review 1.  WD40-Repeat Proteins in Ciliopathies and Congenital Disorders of Endocrine System.

Authors:  Yeonjoo Kim; Soo-Hyun Kim
Journal:  Endocrinol Metab (Seoul)       Date:  2020-09-08
  1 in total

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