A new familial immunodeficiency disorder characterized by severe neutropenia, a defective marrow release mechanism, and hypogammaglobulinemia

Am J Med. 1990 Nov;89(5):663-72. doi: 10.1016/0002-9343(90)90187-i.

Authors

M Wetzler¹, M Talpaz, E S Kleinerman, A King, Y O Huh, J U Gutterman, R Kurzrock

Affiliation

¹ Department of Clinical Immunology, University of Texas, M.D. Anderson Cancer Center, Houston 77030.

PMID: 2239986
DOI: 10.1016/0002-9343(90)90187-i

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't
Review

MeSH terms

Adult
Agammaglobulinemia / genetics*
Agammaglobulinemia / pathology
Bone Marrow / pathology
Bone Marrow Diseases / genetics*
Bone Marrow Diseases / pathology
Female
Hand Dermatoses / genetics
Humans
Immunologic Deficiency Syndromes / genetics*
Immunologic Deficiency Syndromes / pathology
Leukocytes, Mononuclear / pathology
Neutropenia / genetics*
Neutropenia / pathology
Warts / genetics