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Germline Predisposition to Myelodysplastic Syndromes
被引:1
|作者:
Gener-Ricos, Georgina
[1
]
Gerstein, Yoheved S.
[2
]
Hammond, Danielle
[1
]
DiNardo, Courtney D.
[1
,3
]
机构:
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX USA
[2] Univ Texas MD Anderson Canc Ctr, Clin Canc Genet Program, Houston, TX USA
[3] Dept Leukemia, 1515 Holcombe Blvd,Unit 428, Houston, TX 77030 USA
来源:
关键词:
Bone marrow failure;
familial disorders;
germline predisposition;
hereditary;
myelodysplastic syndromes;
SEVERE CONGENITAL NEUTROPENIA;
FAMILIAL PLATELET DISORDER;
DIAMOND-BLACKFAN ANEMIA;
LI-FRAUMENI SYNDROME;
FANCONI-ANEMIA;
GATA2;
MUTATIONS;
TP53;
MUTATION;
INHERITED THROMBOCYTOPENIA;
CLINICAL CHARACTERISTICS;
AUTOSOMAL-DOMINANT;
D O I:
10.1097/PPO.0000000000000660
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
While germline predisposition to myelodysplastic syndromes is well-established, knowledge has advanced rapidly resulting in more cases of inherited hematologic malignancies being identified. Understanding the biological features and main clinical manifestations of hereditary hematologic malignancies is essential to recognizing and referring patients with myelodysplastic syndrome, who may underlie inherited predisposition, for appropriate genetic evaluation. Importance lies in individualized genetic counseling along with informed treatment decisions, especially with regard to hematopoietic stem cell transplant-related donor selection. Future studies will improve comprehension of these disorders, enabling better management of affected patients and their families.
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页码:143 / 151
页数:9
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