Literature DB >> 8319705

A kindred with Griscelli disease: spectrum of neurological involvement.

H Hurvitz1, R Gillis, S Klaus, A Klar, F Gross-Kieselstein, E Okon.   

Abstract

We report four members of a highly consanguineous family with silver-grey pigmentation of hair, two of whom had skin histology compatible with Griscelli disease. Unlike previously reported patients, they did not suffer from recurrent infections. In addition, there was a spectrum of neurological involvement varying from mild cognitive delay with a convulsive disorder in one patient, to a fatal degenerative course in three others. One patient developed a prolonged febrile illness with histological evidence of florid lymphoid hyperplasia.

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Year:  1993        PMID: 8319705     DOI: 10.1007/bf01955897

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  15 in total

1.  Differential effect of isolated placental isoferritins on in vitro T-lymphocyte function.

Authors:  Y Matzner; A M Konijn; Z Shlomai; H Ben-Bassat
Journal:  Br J Haematol       Date:  1985-03       Impact factor: 6.998

2.  Acyclovir in accelerated phase of Chediak-Higashi syndrome.

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3.  Detection by immunochemical techniques of cell surface markers on epidermal Langerhans cells.

Authors:  P R Bergstresser; D V Juarez
Journal:  Methods Enzymol       Date:  1984       Impact factor: 1.600

4.  Human granulocyte-macrophage colony-stimulating factor is a neutrophil activator.

Authors:  R H Weisbart; D W Golde; S C Clark; G G Wong; J C Gasson
Journal:  Nature       Date:  1985 Mar 28-Apr 3       Impact factor: 49.962

5.  Effect of exogenous recombinant human granulocyte and granulocyte-macrophage colony-stimulating factor on neutrophil function following allogeneic bone marrow transplantation.

Authors:  I Fabian; Y Kletter; I Bleiberg; M Gadish; E Naparsteck; S Slavin
Journal:  Exp Hematol       Date:  1991-10       Impact factor: 3.084

6.  Lymphokine-activated killer (LAK) cells. Analysis of factors relevant to the immunotherapy of human cancer.

Authors:  A A Rayner; E A Grimm; M T Lotze; E W Chu; S A Rosenberg
Journal:  Cancer       Date:  1985-03-15       Impact factor: 6.860

7.  Correction of leukocyte function in Chediak-Higashi syndrome by ascorbate.

Authors:  L A Boxer; A M Watanabe; M Rister; H R Besch; J Allen; R L Baehner
Journal:  N Engl J Med       Date:  1976-11-04       Impact factor: 91.245

8.  Mutations affecting pigmentation in man: I. Neuroectodermal melanolysosomal disease.

Authors:  B R Elejalde; J Holguin; A Valencia; E F Gilbert; J Molina; G Marin; L A Arango
Journal:  Am J Med Genet       Date:  1979

9.  Epstein-Barr virus infections and DNA hybridization studies in posttransplantation lymphoma and lymphoproliferative lesions: the role of primary infection.

Authors:  M Ho; G Miller; R W Atchison; M K Breinig; J S Dummer; W Andiman; T E Starzl; R Eastman; B P Griffith; R L Hardesty
Journal:  J Infect Dis       Date:  1985-11       Impact factor: 5.226

10.  A syndrome associating partial albinism and immunodeficiency.

Authors:  C Griscelli; A Durandy; D Guy-Grand; F Daguillard; C Herzog; M Prunieras
Journal:  Am J Med       Date:  1978-10       Impact factor: 4.965

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  12 in total

1.  Cellular and clinical report of new Griscelli syndrome type III cases.

Authors:  Wendy Westbroek; Aharon Klar; Andrew R Cullinane; Shira G Ziegler; Haggit Hurvitz; Ashraf Ganem; Kirkland Wilson; Heidi Dorward; Marjan Huizing; Haled Tamimi; Igor Vainshtein; Yackov Berkun; Moran Lavie; William A Gahl; Yair Anikster
Journal:  Pigment Cell Melanoma Res       Date:  2011-10-03       Impact factor: 4.693

2.  Molecular genetic dissection of mouse unconventional myosin-VA: tail region mutations.

Authors:  J D Huang; V Mermall; M C Strobel; L B Russell; M S Mooseker; N G Copeland; N A Jenkins
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

3.  Griscelli syndrome type 2: a novel mutation in RAB27A gene with different clinical features in 2 siblings: a diagnostic conundrum.

Authors:  Kirtisudha Mishra; Shilpy Singla; Suvasini Sharma; Renu Saxena; Vineeta Vijay Batra
Journal:  Korean J Pediatr       Date:  2014-02-24

4.  Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2B.

Authors:  Fang-Shin Nian; Lei-Li Li; Chih-Ya Cheng; Pei-Chun Wu; You-Tai Lin; Cheng-Yung Tang; Bo-Shiun Ren; Chin-Yin Tai; Ming-Ji Fann; Lung-Sen Kao; Chen-Jee Hong; Jin-Wu Tsai
Journal:  Mol Neurobiol       Date:  2019-02-05       Impact factor: 5.590

5.  Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

Authors:  Ozden Sanal; Fúgen Ersoy; Ilhan Tezcan; Ayşe Metin; Leman Yel; Gaël Ménasché; Aytemiz Gürgey; Izzet Berkel; Geneviève de Saint Basile
Journal:  J Clin Immunol       Date:  2002-07       Impact factor: 8.317

6.  Griscelli syndrome.

Authors:  Sanjeev Rath; Vivek Jain; R K Marwaha; Amita Trehan; L S Rajesh; Vijay Kumar
Journal:  Indian J Pediatr       Date:  2004-02       Impact factor: 1.967

7.  Evidence that Griscelli syndrome with neurological involvement is caused by mutations in RAB27A, not MYO5A.

Authors:  Yair Anikster; Marjan Huizing; Paul D Anderson; Diana L Fitzpatrick; Aharon Klar; Eva Gross-Kieselstein; Yackov Berkun; Gila Shazberg; William A Gahl; Haggit Hurvitz
Journal:  Am J Hum Genet       Date:  2002-06-07       Impact factor: 11.025

8.  A novel missense mutation (G43S) in the switch I region of Rab27A causing Griscelli syndrome.

Authors:  Wendy Westbroek; Maya Tuchman; Bradford Tinloy; Olivier De Wever; Thierry Vilboux; Jens M Hertz; Henrik Hasle; Carsten Heilmann; Amanda Helip-Wooley; Robert Kleta; William A Gahl
Journal:  Mol Genet Metab       Date:  2008-04-07       Impact factor: 4.797

9.  The role of the COOH terminus of Sec2p in the transport of post-Golgi vesicles.

Authors:  N B Elkind; C Walch-Solimena; P J Novick
Journal:  J Cell Biol       Date:  2000-04-03       Impact factor: 10.539

10.  Silvery grey hair: clue to diagnose immunodeficiency.

Authors:  Ms Sahana; S Sacchidanand; R Hiremagalore; Gs Asha
Journal:  Int J Trichology       Date:  2012-04
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