1.Genetic analysis of an individual with a fragile site at 16q22.
Minjie SHAO ; Yun WANG ; Chan TIAN ; Liping JIAO ; Ping LIU
Chinese Journal of Medical Genetics 2021;38(4):380-382
OBJECTIVE:
To analyze a patient with infertility and a fragile site found at 16q22 by using cytogenetic methods.
METHODS:
Peripheral blood sample was taken from the patient and subjected to chromosomal karyotyping and single nucleotide polymorphism microarray (SNP-array) analysis.
RESULTS:
The patient was found to be a mosaicism for a fragile site at 16q22, which has a variable morphology and cannot be induced by folic acid treatment. No abnormality was found by SNP-array analysis.
CONCLUSION
A rare fragile site, which can be induced without folic acid treatment, has been identified at 16q22. The strategy of assisted reproduction for such individuals is yet to be explored.
Chromosome Fragile Sites
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Chromosome Fragility
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Chromosomes, Human, Pair 16
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Genetic Testing
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Humans
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Karyotyping
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Mosaicism
2.The Expression of Folate Sensitive Fragile Sites in Patients with Bipolar Disorder.
Osman DEMIRHAN ; Deniz TASTEMIR ; Yasar SERTDEMIR
Yonsei Medical Journal 2009;50(1):137-141
PURPOSE: Genetic factors are known to be important in the etiology of bipolar disorder (BD). The fragile sites (FSs) are a very interesting subject for the study of clinical disorders. The aim of this study was to evaluate fragile sites seen in patients with bipolar disorder and find a correlation between some fragile sites and bipolar disorder. PATIENTS AND METHODS: The frequencies of folate sensitive FSs were compared in short-term whole blood cultures from bipolar patients and from normal individuals. RESULTS: The rate of FS expression in the patients was considerably higher than in the controls (p < 0.001). Several chromosome regions including 1p36, 1q21, 1q32, 3p25, 7q22, 7q32, 11q23, 12q24, 13q32, 14q24, Xp22 and Xq26 were represented considerably more often in the patients than in the controls (p value between 0.001 to 0.036). Among these FSs, the sites 1p36, 1q21, 3p25, 7q22, 7q32, and 14q24 were not observed in other studies. CONCLUSION: These regions can be the most active of hot spots in the genomes of bipolar patients, and may harbor important genes associated with BD.
Adolescent
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Adult
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Bipolar Disorder/*genetics
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Chromosome Fragile Sites/drug effects/*genetics
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Chromosome Fragility/drug effects/*genetics
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Chromosomes, Human/*genetics
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Cytogenetics
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Female
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Folic Acid/pharmacology
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Genetic Predisposition to Disease
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Humans
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Male
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Middle Aged
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Young Adult