Erythrophagocytic Lymphohistiocytosis: A Case Report-Reference-Cited by-同舟云学术

Erythrophagocytic Lymphohistiocytosis: A Case Report

Published:1988-01 Issue:1 Volume:8 Page:56-60
ISSN:0256-4947
Container-title:Annals of Saudi Medicine
language:en
Short-container-title:Ann Saudi Med

Author:

Issa Abdul Rahman A.¹,Teebi Ahmad S.²,Issa Mohammed A.³,Ahmad Mahmoud S.⁴,Voncina Drago⁴,Al-Rashied Abdullah A.⁵

Affiliation:

1. Senior Registrar, Department of Pediatrics, Sabah Hospital, P.O. Box 4078, Safat 13041, Kuwait

2. Senior Registrar, Medical Genetics Centre, Sabah Hospital

3. Head of Unit, Department of Pediatric Surgery, Ibn Sina Hospital, Safat, Kuwait

4. Consultant, Department of Pathology, Sabah Hospital

5. Professor, Head of Department, Department of Pediatrics, Sabah Hospital

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference23 articles.

1. McKusick VA. Mendelian inheritance in man: catalog of autosomal dominant autosomal recessive and X-linked phenotypes. 7th ed. Baltimore: Johns Hopkins University Press; 1986:1233–4.

2. Familial hemophagocytic reticulosis;Farquhar JW;Arch Dis Child,1952

3. Familial erythrophagocytic reticulosis: complete response to combination chemotherapy;Delaney MM;Arch Dis Child,1984

4. Neuropathology of familial erythrophagocytic lymphohistocytosis: six cases and review of the literature;Akima M;Hum Pathol,1984

5. Genetic analysis of familial erythrophagocytic lymphohistiocytosis;Gencik A;Eur J Pediatr,1984

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1. Autosomal recessive disorders among Arabs: an overview from Kuwait.;Journal of Medical Genetics;1994-03-01