Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency. Issue 9 (25th August 2020)
- Record Type:
- Journal Article
- Title:
- Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency. Issue 9 (25th August 2020)
- Main Title:
- Biallelic variants in BRCA1 gene cause a recognisable phenotype within chromosomal instability syndromes reframed as BRCA1 deficiency
- Authors:
- Chirita-Emandi, Adela
Andreescu, Nicoleta
Popa, Cristina
Mihailescu, Alexandra
Riza, Anca-Lelia
Plesea, Razvan
Ioana, Mihai
Arghirescu, Smaranda
Puiu, Maria - Abstract:
- Abstract : Pathogenic variants in BRCA1 gene in heterozygous state are known to be associated with breast-ovarian cancer susceptibility; however, biallelic variants cause a phenotype recognised as Fanconi anaemia complementation group S. Due to its rarity, medical management and preventive screening measures are insufficiently understood. Here, we present nine individuals (one new and eight previously presented) with biallelic variants in BRCA1 gene, to delineate clinical features in comparison with other chromosome instability syndromes and understand the patients' health risk. Features seen in these 9 individuals (7 females/2 males) include prenatal and postnatal growth failure (9/9), microcephaly (9/9), hypo/hyperpigmented lesions (9/9), facial dysmorphism (9/9), mild developmental delay (8/9) and early-onset solid tumours (5/9). None presented bone marrow failure or immunodeficiency. Individuals with biallelic variants in BRCA1 also showed chromosomal instability by mitomycin and diepoxybutane test. The phenotype caused by biallelic BRCA1 variants is best framed between Fanconi anaemia and Nijmegen syndrome, yet distinct due to lack of bone marrow failure and immunodeficiency. We hypothesise that disease class should be reframed and medical management in people with biallelic variants in BRCA1 should emphasise on detection of solid tumour development and avoiding exposure to ionising radiation.
- Is Part Of:
- Journal of medical genetics. Volume 58:Issue 9(2021)
- Journal:
- Journal of medical genetics
- Issue:
- Volume 58:Issue 9(2021)
- Issue Display:
- Volume 58, Issue 9 (2021)
- Year:
- 2021
- Volume:
- 58
- Issue:
- 9
- Issue Sort Value:
- 2021-0058-0009-0000
- Page Start:
- 648
- Page End:
- 652
- Publication Date:
- 2020-08-25
- Subjects:
- genetics -- child health -- diagnosis
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/jmedgenet-2020-107198 ↗
- Languages:
- English
- ISSNs:
- 1468-6244
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 25232.xml