Reduced Serum Levels of Anti-Müllerian Hormone in Females With Inherited Bone Marrow Failure Syndromes
Author(s) -
Martha M. Sklavos,
Pamela Stratton,
Neelam Giri,
Blanche P. Alter,
Sharon A. Savage,
Lígia A. Pinto
Publication year - 2014
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2014-2838
Subject(s) - medicine , anti müllerian hormone , fanconi anemia , bone marrow failure , anemia , bone marrow , ovarian reserve , endocrinology , gastroenterology , hormone , cancer , pregnancy , haematopoiesis , stem cell , biology , infertility , biochemistry , genetics , dna repair , gene
Previously, reduced levels of anti-Müllerian hormone (AMH), a circulating marker of ovarian reserve, were found in females with Fanconi anemia (FA). FA, dyskeratosis congenita (DC), and Diamond-Blackfan anemia (DBA) are inherited bone marrow failure syndromes (IBMFS) associated with high risks of bone marrow failure, leukemia, and solid tumors.
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