terminal;
10q deletion;
sex differentiation;
cryptorchidism;
D O I:
10.1159/000030321
中图分类号:
R5 [内科学];
R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号:
1002 ;
100201 ;
摘要:
We report on an infant with terminal deletion of 10q (del10q26.11) presenting with bilateral cryptorchidism. Of 9 males previously reported with terminal deletion of 10q, 1 had an intersex phenotype. and the others all had combinations of cryptorchidism, micropenis, and hypospadias. Terminal deletion of 10q appears to include some genes indispensable for normal male genital development.
机构:
Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
ARUP Labs, 500 Chipeta Way, Salt Lake City, UT 84108 USAUniv Utah, Dept Pathol, Salt Lake City, UT 84112 USA
Herriges, John C.
Dugan, Sarah L.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Utah, Dept Pediat Med Genet, Salt Lake City, UT USAUniv Utah, Dept Pathol, Salt Lake City, UT 84112 USA
Dugan, Sarah L.
Lamb, Allen N.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USA
ARUP Labs, 500 Chipeta Way, Salt Lake City, UT 84108 USAUniv Utah, Dept Pathol, Salt Lake City, UT 84112 USA