Bloom syndrome (Q56897): Difference between revisions

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13 August 2026
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Latest revision as of 04:35, 14 August 2026

Bloom syndrome is a rare autosomal recessive disorder belonging to a group of chromosomal breakage syndromes, and is characterised by marked genetic instability, including a high level of sister chromatid exchanges, associated with a greatly increased predisposition to a wide range of cancers commonly affecting the general population. The constant clinical features of BS are proportionate pre- and postnatal growth retardation and cancer predisposition. Additional clinical features include dolichocephaly, facial sun-sensitive telangiectatic erythema, patchy areas of hyper- and hypopigmentation of the skin and moderate to severe immunodeficiency manifested by recurrent respiratory tract and gastrointestinal infections.
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ID_1838213890
    English
    Bloom syndrome
    Bloom syndrome is a rare autosomal recessive disorder belonging to a group of chromosomal breakage syndromes, and is characterised by marked genetic instability, including a high level of sister chromatid exchanges, associated with a greatly increased predisposition to a wide range of cancers commonly affecting the general population. The constant clinical features of BS are proportionate pre- and postnatal growth retardation and cancer predisposition. Additional clinical features include dolichocephaly, facial sun-sensitive telangiectatic erythema, patchy areas of hyper- and hypopigmentation of the skin and moderate to severe immunodeficiency manifested by recurrent respiratory tract and gastrointestinal infections.

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      CID11:ID_1838213890
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      dki-india-ID_1838213890
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      Concluído
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      13 August 2026
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