GENETIC IMMUNODEFICIENCIES - CUTANEOUS MANIFESTATIONS AND RECENT PROGRESS

被引:17
作者
ARBISER, JL
机构
[1] HARVARD UNIV, SCH MED, BOSTON, MA USA
[2] CHILDRENS HOSP, HOWARD HUGHES MED INST, BOSTON, MA USA
关键词
D O I
10.1016/0190-9622(95)90016-0
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
In recent years, remarkable progress has been made in elucidating the pathophysiology of genetic immunodeficiency disorders. Dermatologic manifestations are prominent in these conditions; because of advances in diagnosis and therapy, patients are living longer, increasing the likelihood that dermatologists will encounter patients with these diseases. The genes of many of these disorders have been cloned, including chronic granulomatous disease, X-linked immunodeficiencies, and myeloperoxidase deficiency. Understanding the regulation and function of these genes will not only affect patients with these rare disorders, but may provide an insight into common dermatologic conditions, such as eczema and cutaneous infection. Diagnosis, dermatologic manifestations, and therapy are discussed.
引用
收藏
页码:82 / 89
页数:8
相关论文
共 73 条
[1]   CD40 LIGAND GENE DEFECTS RESPONSIBLE FOR X-LINKED HYPER-IGM SYNDROME [J].
ALLEN, RC ;
ARMITAGE, RJ ;
CONLEY, ME ;
ROSENBLATT, H ;
JENKINS, NA ;
COPELAND, NG ;
BEDELL, MA ;
EDELHOFF, S ;
DISTECHE, CM ;
SIMONEAUX, DK ;
FANSLOW, WC ;
BELMONT, J ;
SPRIGGS, MK .
SCIENCE, 1993, 259 (5097) :990-993
[2]   THE CD40 LIGAND, GP39, IS DEFECTIVE IN ACTIVATED T-CELLS FROM PATIENTS WITH X-LINKED HYPER-IGM SYNDROME [J].
ARUFFO, A ;
FARRINGTON, M ;
HOLLENBAUGH, D ;
LI, X ;
MILATOVICH, A ;
NONOYAMA, S ;
BAJORATH, J ;
GROSMAIRE, LS ;
STENKAMP, R ;
NEUBAUER, M ;
ROBERTS, RL ;
NOELLE, RJ ;
LEDBETTER, JA ;
FRANCKE, U ;
OCHS, HD .
CELL, 1993, 72 (02) :291-300
[3]  
BABIOR BM, 1990, SEMIN HEMATOL, V27, P247
[4]   QUANTITATIVE NITROBLUE TETRAZOLIUM TEST IN CHRONIC GRANULOMATOUS DISEASE [J].
BAEHNER, RL ;
NATHAN, DG .
NEW ENGLAND JOURNAL OF MEDICINE, 1968, 278 (18) :971-&
[5]  
BARAK Y, 1987, AM J PEDIAT HEMATOL, V9, P42
[6]   FATAL ECHO 24 INFECTION IN A PATIENT WITH HYPOGAMMAGLOBULINEMIA - RELATIONSHIP TO DERMATOMYOSITIS-LIKE SYNDROME [J].
BARDELAS, JA ;
WINKELSTEIN, JA ;
SETO, DSY ;
TSAI, T ;
ROGOL, AD .
JOURNAL OF PEDIATRICS, 1977, 90 (03) :396-399
[7]   TOPOGRAPHICAL ANALYSIS OF THE G-VIRION OF ALEUTIAN MINK DISEASE PARVOVIRUS WITH MONOCLONAL-ANTIBODIES [J].
BARNARD, DL ;
JOHNSON, FB .
ARCHIVES OF VIROLOGY, 1992, 127 (1-4) :271-289
[8]   MUTATIONS IN THE DNA LIGASE-I GENE OF AN INDIVIDUAL WITH IMMUNODEFICIENCIES AND CELLULAR-HYPERSENSITIVITY TO DNA-DAMAGING AGENTS [J].
BARNES, DE ;
TOMKINSON, AE ;
LEHMANN, AR ;
WEBSTER, ADB ;
LINDAHL, T .
CELL, 1992, 69 (03) :495-503
[9]   CHRONIC GRANULOMATOUS DISEASE OF CHILDHOOD - SUPERFICIAL PYODERMA AS A MAJOR DERMATOLOGIC MANIFESTATION [J].
BASS, LJ ;
VOORHEES, JJ ;
TANNER, MH ;
DUBIN, HV .
ARCHIVES OF DERMATOLOGY, 1972, 106 (01) :68-&
[10]  
BERNHARD JD, 1987, CLIN DERMATOL WORLD, P3