ISOLATED CONGENITAL ATRICHIA IN AN OMANI KINDRED

被引:8
作者
KENUE, RK [1 ]
ALDHAFRI, KS [1 ]
机构
[1] SULTAN QABOOS UNIV,COLL SCI,DEPT BIOL,MASQAT,OMAN
关键词
CONGENITAL ATRICHIA; ALOPECIA; HAIR DISORDER; RECESSIVE HAIRLESSNESS;
D O I
10.1159/000247092
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Congenital atrichia may occur isolated or with associated defects. The isolated variant is especially uncommon. Sporadic and familial cases have been rarely reported. We present a large inbred kindred from Oman where 22 affected members with this disorder were found over six generations. The male-to-female ratio was 1:1.4. No associated ectodermal or other defects were noted. A typical autosomal recessive mode of inheritance was documented. Though inbreeding was high, anticipated quasidominance was observed only once.
引用
收藏
页码:72 / 75
页数:4
相关论文
共 18 条
  • [1] ANALYSIS OF HAIR FROM ALOPECIA CONGENITA
    BADEN, HP
    KUBILUS, J
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1980, 3 (06) : 623 - 626
  • [2] BENTLEYPHILLIPS B, 1979, BRIT J DERMATOL, V101, P331
  • [3] BERTOLINO AP, 1987, DERMATOLOGY GENERAL, P627
  • [4] BIRKE G, 1954, Arch Klin Exp Dermatol, V197, P322, DOI 10.1007/BF00361701
  • [5] HERITABLE DISORDERS OF HAIR
    BIRNBAUM, PS
    BADEN, HP
    [J]. DERMATOLOGIC CLINICS, 1987, 5 (01) : 137 - 153
  • [6] CANTU JM, 1980, CLIN GENET, V17, P209
  • [7] Ebling FJG, 1986, TXB DERMATOLOGY, P1937
  • [8] LINN H W, 1964, Aust J Dermatol, V7, P223, DOI 10.1111/j.1440-0960.1964.tb01355.x
  • [9] LUNDBACK H, 1944, ACTA DERM-VENEREOL, V25, P189
  • [10] ALOPECIA - SYNDROMES OF GENETIC SIGNIFICANCE
    MULLER, SA
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1973, 60 (06) : 475 - 492