A functioning eccrine hamartoma associated with Down's syndrome (46,xx,-21,+t(21q21q)

被引:0
|
作者
Nightingale, KJ [1 ]
Newman, P [1 ]
Davies, MG [1 ]
机构
[1] Derriford Hosp, Plymouth PL6 8DH, Devon, England
关键词
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Pure eccrine hamartomas are very rare, and commonly present as localized areas of hyperhidrosis in normal looking skin. We describe a case of bilateral functioning eccrine hamartomas with macroscopically abnormal features in association with Down's syndrome.
引用
收藏
页码:264 / 266
页数:3
相关论文
共 50 条
  • [1] PARENTAL MOSAICISM AS A CAUSE OF DOWN SYNDROME - REPORT OF 46,XX-46,XX,-21,+T(21Q21Q) MOTHER AND 46,XY,+21,+T(21Q21Q) CHILD
    PRIEST, JH
    BRANTLEY, KE
    BLACKSTON, RD
    JOURNAL OF PEDIATRICS, 1977, 90 (05): : 786 - 788
  • [2] PRENATAL-DIAGNOSIS OF MOSAICISM 46,XX/46,XX,-21,+T(21Q21Q)
    LONG, WS
    MENNUTI, MT
    EMANUEL, BS
    ZACKAI, EH
    PRENATAL DIAGNOSIS, 1984, 4 (01) : 73 - 77
  • [3] DOWNS-SYNDROME ASSOCIATED WITH 2 ROBERTSONIAN TRANSLOCATIONS, 45,XX,-15,-21,+T(15Q21Q) AND 46,XX,-21,+T(21Q21Q)
    ATKINS, L
    BARTSOCAS, CS
    JOURNAL OF MEDICAL GENETICS, 1974, 11 (03) : 306 - 309
  • [4] CASE OF ATYPICAL DOWNS-SYNDROME WITH MOSAIC 46,XX-46,XX-21+T(21Q21Q)
    HORNSTEIN, L
    SOUKUP, S
    CLINICAL GENETICS, 1976, 10 (02) : 77 - 81
  • [5] RECURRENCE RISK IN DENOVO 21Q21Q TRANSLOCATION DOWN SYNDROME
    HALL, BD
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 22 (02): : 417 - 418
  • [6] T(21Q21Q)-R[T(21Q21Q)] MOSAIC IN 2 UNRELATED PATIENTS WITH MILD STIGMATA OF DOWNS-SYNDROME
    DALLAPICCOLA, B
    BIANCO, I
    BRINCHI, V
    SANTULLI, B
    SCARANO, G
    SICOLO, A
    STABILE, M
    VENTRUTO, V
    ANNALES DE GENETIQUE, 1982, 25 (01): : 56 - 58
  • [7] TRISOMY-21 BY MIRROR DUPLICATION 46,XX,PSU DIC(21)TER REA (21Q21Q)
    TURLEAU, C
    ROUBIN, M
    CHAVINCOLIN, F
    GROUCHY, JD
    ANNALES DE GENETIQUE, 1980, 23 (03): : 187 - 189
  • [8] T(21Q21Q) RING CHROMOSOME
    ORYE, E
    CRAEN, M
    HUMAN HEREDITY, 1974, 24 (03) : 253 - 258
  • [9] MOSAIC DOWNS-SYNDROME WITH DENOVO 45,XX,-21,-22,+T(21Q-22Q)/46,XX,-21,+T(21Q-21Q) REARRANGEMENT
    THARAPEL, AT
    REDHEENDRAN, R
    MANKINEN, CB
    KUKOLICH, MK
    JOURNAL OF MEDICAL GENETICS, 1984, 21 (05) : 391 - 395
  • [10] DENOVO 21Q21Q WITH 21P21P PRESERVED IN MAJORITY OF CELLS IN DOWN SYNDROME
    FRIED, K
    ROSENBLATT, M
    GOLDBERG, MD
    AMERICAN JOURNAL OF HUMAN GENETICS, 1982, 34 (06) : A125 - A125