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PMID: 457130 Published · ppublish English Case Reports Journal Article

A case of long arm deletion of the X chromosome in a patient with secondary amenorrhea.

Human genetics ·Vol. 48 ·No. 1 ·1979-04-17 ·Pages 139-42

Branković S, Laća Z, Dramusić V, Ivanović M, Morić-Petrović S

Abstract

This paper presents the clinical and cytogenetic findings in a female patient with secondary amenorrhea and normal phenotype. Some difficulties related to karyotype-phenotype correlation are discussed.

MeSH Terms
Adult Amenorrhea/genetics Chromosome Deletion Female Humans Karyotyping Phenotype Sex Chromatin Sex Chromosomes Turner Syndrome/diagnosis X Chromosome
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Branković S
Laća Z
Dramusić V
Ivanović M
Morić-Petrović S
References (7)
7 references, click to expand
  1. Deletion mapping of the human X chromosome.
    Hereditas. 1975;80(1):113-20 PMID: 1141012
  2. Letter: X long-arm deletion with features of Turner's syndrome.
    Lancet. 1974 Aug 17;2(7877):403-4 PMID: 4137037
  3. Xq- Turner's syndrome: reconsideration of hypothesis that Xp- causes somatic features in Turner's syndrome.
    J Med Genet. 1970 Mar;7(1):1-4 PMID: 5480961
  4. Somatic stigmata of Turner's syndrome in a patient with 46,XXq-.
    J Med Genet. 1971 Sep;8(3):358-63 PMID: 5097143
  5. Fluorescence and autoradiographic studies in patients with Turner's syndrome and 46,XXp- and 46,XXq- karyotypes.
    J Med Genet. 1973 Dec;10(4):350-5 PMID: 4129970
  6. [Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine].
    C R Acad Sci Hebd Seances Acad Sci D. 1973 Jun 13;276(24):3179-81 PMID: 4125131
  7. A rapid banding technique for human chromosomes.
    Lancet. 1971 Oct 30;2(7731):971-2 PMID: 4107917
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
DOI
10.1007/BF00273289
Published
1979-04-17
Pages
139-42
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
External Links
PubMed source DOI: 10.1007/BF00273289 View journal details
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