Literature DB >> 8030398

Adult Chédiak-Higashi syndrome presenting as parkinsonism and dementia.

E Uyama1, T Hirano, K Ito, H Nakashima, M Sugimoto, M Naito, M Uchino, M Ando.   

Abstract

Chédiak-Higashi syndrome (CHS) in children can be a fatal disease. We describe the oldest known CHS patient first seen with a neurologic disorder in early adult life. From the age of 22, this 39-year-old woman developed mental deterioration, parkinsonism including resting tremor at the tongue, mandible, and hands, oculogyric crisis, muscular atrophy of limbs, and loss of tendon reflexes. MRI showed marked temporal dominant brain atrophy and diffuse spinal cord atrophy. Partial albinism, pan-leukocytic giant granules, and profoundly decreased NK-cell activity were compatible with childhood CHS, but apparently normal neutrophil function prolonged her survival. Stimulated proliferation of lymphocytes was less than 40% that of normal controls.

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Year:  1994        PMID: 8030398     DOI: 10.1111/j.1600-0404.1994.tb01657.x

Source DB:  PubMed          Journal:  Acta Neurol Scand        ISSN: 0001-6314            Impact factor:   3.209


  12 in total

Review 1.  [Chediak-Higashi syndrome].

Authors:  J Wolf; C Jacobi; H Breer; A Grau
Journal:  Nervenarzt       Date:  2006-02       Impact factor: 1.214

Review 2.  Albinism: modern molecular diagnosis.

Authors:  S M Carden; R E Boissy; P J Schoettker; W V Good
Journal:  Br J Ophthalmol       Date:  1998-02       Impact factor: 4.638

3.  Chediak-Higashi syndrome presenting as young-onset levodopa-responsive parkinsonism.

Authors:  Vikas Bhambhani; Wendy J Introne; Codrin Lungu; Andrew Cullinane; Camilo Toro
Journal:  Mov Disord       Date:  2013-02       Impact factor: 10.338

4.  Parkinsonism and Other Movement Disorders Associated with Chediak-Higashi Syndrome: Case Report and Systematic Literature Review.

Authors:  Bettina Balint; Kailash P Bhatia
Journal:  Mov Disord Clin Pract       Date:  2015-01-14

Review 5.  Genetic defects in Chediak-Higashi syndrome and the beige mouse.

Authors:  R A Spritz
Journal:  J Clin Immunol       Date:  1998-03       Impact factor: 8.317

6.  Neurologic involvement in patients with atypical Chediak-Higashi disease.

Authors:  Wendy J Introne; Wendy Westbroek; Andrew R Cullinane; Catherine A Groden; Vikas Bhambhani; Gretchen A Golas; Eva H Baker; Tanya J Lehky; Joseph Snow; Shira G Ziegler; David R Adams; Heidi M Dorward; Richard A Hess; Marjan Huizing; William A Gahl; Camilo Toro
Journal:  Neurology       Date:  2016-03-04       Impact factor: 9.910

7.  Lyst mutation in mice recapitulates iris defects of human exfoliation syndrome.

Authors:  Colleen M Trantow; Mao Mao; Greg E Petersen; Erin M Alward; Wallace L M Alward; John H Fingert; Michael G Anderson
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-11-21       Impact factor: 4.799

Review 8.  A Practical Approach to Early-Onset Parkinsonism.

Authors:  Giulietta M Riboldi; Emanuele Frattini; Edoardo Monfrini; Steven J Frucht; Alessio Di Fonzo
Journal:  J Parkinsons Dis       Date:  2022       Impact factor: 5.568

Review 9.  Towards the targeted management of Chediak-Higashi syndrome.

Authors:  Maria L Lozano; Jose Rivera; Isabel Sánchez-Guiu; Vicente Vicente
Journal:  Orphanet J Rare Dis       Date:  2014-08-18       Impact factor: 4.123

10.  Atypical Chédiak-Higashi syndrome with attenuated phenotype: three adult siblings homozygous for a novel LYST deletion and with neurodegenerative disease.

Authors:  James D Weisfeld-Adams; Lakshmi Mehta; Janet C Rucker; Francine R Dembitzer; Arnold Szporn; Fred D Lublin; Wendy J Introne; Vikas Bhambhani; Michael C Chicka; Catherine Cho
Journal:  Orphanet J Rare Dis       Date:  2013-03-22       Impact factor: 4.123

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