Literature DB >> 10653334

Accelerated phase in partial albinism with immunodeficiency (Griscelli syndrome): genetics and stem cell transplantation in a 2-month-old girl.

F A Baumeister1, D Stachel, F Schuster, I Schmid, M Schaller, H Wolff, M Weiss, B H Belohradsky.   

Abstract

UNLABELLED: A 2-month-old girl presented with fever, hepatosplenomegaly, pancytopenia, hypertriglyceridaemia and silvery-greyish hair, suggesting the diagnosis of Griscelli syndrome (partial albinism with immunodeficiency). This diagnosis was confirmed by the characteristic agglomeration of melanin in the hair shaft and accumulation of melanosomes in melanocytes of the skin. The patient was homozygous for polymorphic markers around the myosin-Va gene on chromosome 15q21, which co-localize to the Griscelli disease locus. Natural-killer cells were in the lower range. The stimulation of lymphocytes with antigen and mitogen was normal. The patient's accelerated phase, characterized by haemophagocytosis was treated with prednisolone, rabbit anti-thymocyte globulins, and intrathecal methotrexate. Remission was maintained with cyclosporin A until HLA-compatible peripheral blood stem cell transplantation from her mother.
CONCLUSION: The silvery-greyish hair associated with fever, pancytopenia and hypertriglyceridaemia is the clue to early diagnosis of Griscelli syndrome and important to prevent death before stem cell transplantation.

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Year:  2000        PMID: 10653334     DOI: 10.1007/pl00013808

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


  5 in total

1.  Analysis of RAB27A gene in griscelli syndrome type 2: novel mutations including a deletion hotspot.

Authors:  Setareh Mamishi; Mohammad Hossein Modarressi; Babak Pourakbari; Banafshe Tamizifar; Fatemeh Mahjoub; Alireza Fahimzad; Soheila Alyasin; Mohamad Hassan Bemanian; Amir Ali Hamidiyeh; Mohammad Reza Fazlollahi; Mahmoud Reza Ashrafi; Anna Isaeian; Ghamartaj Khotaei; Mehdi Yeganeh; Nima Parvaneh
Journal:  J Clin Immunol       Date:  2008-03-19       Impact factor: 8.317

2.  [Hereditary pigmentary disorders].

Authors:  K Giehl; M Braun-Falco
Journal:  Hautarzt       Date:  2010-07       Impact factor: 0.751

3.  Acute Phase Reaction after Femur Fracture in a Child with Griscelli Syndrome.

Authors:  İrfan Güngör; Akif Muhtar Öztürk; Kadir Kaya; Hülya Çelebi; Bahadır Kösem
Journal:  Turk J Anaesthesiol Reanim       Date:  2014-03-11

4.  Development, characterization, and hematopoietic differentiation of Griscelli syndrome type 2 induced pluripotent stem cells.

Authors:  Gülen Güney-Esken; Özgür Doğuş Erol; Burcu Pervin; Gülben Gürhan Sevinç; Tamer Önder; Elif Bilgiç; Petek Korkusuz; Ayşen Günel-Özcan; Duygu Uçkan-Çetinkaya; Fatima Aerts-Kaya
Journal:  Stem Cell Res Ther       Date:  2021-05-13       Impact factor: 6.832

5.  Spectrum of primary immunodeficiency disorders in Sri Lanka.

Authors:  Nilhan Rajiva de Silva; Sepali Gunawardena; Damayanthi Rathnayake; Geethani Devika Wickramasingha
Journal:  Allergy Asthma Clin Immunol       Date:  2013-12-27       Impact factor: 3.406

  5 in total

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