Abstract
A male child and his mother who are nullisomic and monosomic, respectively, for the distal portion of Xp because of an unbalanced X-Y translocation were tested for steroid sulfatase activity after clinical examination had yielded evidence for ichthyosis in the boy. Deficiency of steroid sulfatase was found in the male patient, while in his mother enzyme levels were in the heterozygous range. These results, based on cytogenetic evidence obtained with an elongation technique, indicate that the STS locus is at Xp 223.
MeSH Terms
Adult
Child, Preschool
Chromosome Deletion
Chromosome Mapping
Female
Genetic Linkage
Heterozygote
Humans
Ichthyosis/genetics
Male
Sex Chromosomes
Steryl-Sulfatase
Sulfatases/deficiency,genetics
Translocation, Genetic
X Chromosome
Chemicals
Sulfatases
Steryl-Sulfatase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Tiepolo L
Zuffardi O
Fraccaro M
di Natale D
Gargantini L
Müller C R
Ropers H H
References (7)
7 references, click to expand
-
Clinical and biochemical investigations on patients with partial deficiency of placental steroid sulfatase.
Hum Genet. 1979 Jan 25;46(2):199-207
PMID: 422203
-
X-linked steroid sulfatase: evidence for different gene-dosage in males and females.
Hum Genet. 1980;54(2):197-9
PMID: 6930360
-
Regional assignment of the gene locus for steroid sulfatase.
Hum Genet. 1980;54(2):201-4
PMID: 6985463
-
Nullisomy for the distal portion of Xp in a male child with a X/Y translocation.
Hum Genet. 1977 Dec 23;39(3):277-81
PMID: 598835
-
X-autosome translocations: a review.
Birth Defects Orig Artic Ser. 1978;14(6C):219-47
PMID: 365268
-
Regional assignment of the steroid sulfatase-X-linked ichthyosis locus: implications for a noninactivated region on the short arm of human X chromosome.
Proc Natl Acad Sci U S A. 1979 Nov;76(11):5779-83
PMID: 293682
-
Mechanisms and evolutionary origins of variable X-chromosome activity in mammals.
Proc R Soc Lond B Biol Sci. 1974 Nov 5;187(1088):243-68
PMID: 4154449