NOONANS-SYNDROME IN ASSOCIATION WITH ACUTE-LEUKEMIA

被引:21
作者
JOHANNES, JM
GARCIA, ER
DEVAAN, GAM
WEENING, RS
机构
[1] UNIV AMSTERDAM,ACAD MED CTR,EMMA CHILDRENS HOSP,DEPT PEDIAT,1105 AZ AMSTERDAM,NETHERLANDS
[2] ACAD HOSP NYMEGEN,DEPT PEDIAT,AMSTERDAM,NETHERLANDS
[3] UNIV AMSTERDAM,EXPTL & CLIN IMMUNOL LAB,AMSTERDAM,NETHERLANDS
关键词
ACUTE LEUKEMIA; ACUTE LYMPHATIC LEUKEMIA; ACUTE MYELOID LEUKEMIA; NOONANS SYNDROME;
D O I
10.3109/08880019509030771
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Noonan's syndrome (NS) is a syndrome with multiple congenital anomalies, characterized by craniofacial anomalies, congenital heart disease, skeletal and genital abnormalities, and mild mental retardation. Chromosomal abnormalities have been found in only a few cases. The combination of NS and acute leukemia has been reported in only three cases. Two additional cases are described here.
引用
收藏
页码:571 / 575
页数:5
相关论文
共 15 条
  • [1] NOONAN SYNDROME - THE CHANGING PHENOTYPE
    ALLANSON, JE
    HALL, JG
    HUGHES, HE
    PREUS, M
    WITT, RD
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 507 - 514
  • [2] NOONAN PHENOTYPE ASSOCIATED WITH NEUROFIBROMATOSIS
    ALLANSON, JE
    HALL, JG
    VANALLEN, MI
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 457 - 462
  • [3] NOONANS-SYNDROME AND ACUTE LYMPHOBLASTIC-LEUKEMIA
    ATTARDMONTALTO, SP
    KINGSTON, JE
    EDEN, T
    [J]. MEDICAL AND PEDIATRIC ONCOLOGY, 1994, 23 (04): : 391 - 392
  • [4] UNIFYING LINK BETWEEN NOONANS AND LEOPARD SYNDROMES
    BLIEDEN, LC
    SCHNEEWEISS, A
    SHEMTOV, A
    FEIGEL, A
    NEUFELD, HN
    [J]. PEDIATRIC CARDIOLOGY, 1983, 4 (02) : 168 - 169
  • [5] CHRONIC MYELOGENOUS LEUKEMIA AS A MODEL FOR THE GENETIC-BASIS OF CANCER
    CANNISTRA, SA
    [J]. HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 1990, 4 (02) : 337 - 357
  • [6] Chery M., 1993, Genetic Counseling, V4, P113
  • [7] NO EVIDENCE FOR LINKAGE TO THE TYPE-1 OR TYPE-2 NEUROFIBROMATOSIS LOCI IN NOONAN SYNDROME FAMILIES
    FLINTOFF, WF
    BAHUAU, M
    LYONNET, S
    GILGENKRANTZ, S
    LACOMBE, D
    MARCON, F
    LEVILLIERS, J
    KACHANER, J
    MUNNICH, A
    LEMERRER, M
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1993, 46 (06): : 700 - 705
  • [8] NOONANS SYNDROME - A CASE WITH ELEVATED SERUM ALKALINE PHOSPHATASE LEVELS AND MALIGNANT SCHWANNOMA OF LEFT FOREARM
    KAPLAN, MS
    OPITZ, JM
    GOSSET, FR
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1968, 116 (04): : 359 - &
  • [9] KRISHNAN EU, 1978, PEDIATRICS, V61, P898
  • [10] NOONAN SYNDROME - A REVIEW
    MENDEZ, HMM
    OPITZ, JM
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (03): : 493 - 506