Rare Diseases Symptoms Automatic Extraction

Free proximal trisomy 21 in the mother and malformation syndrome in the son.

[monosomy 21]

We report on a new case of duplication of the proximal part of the long arm of chromosome 21. The proposita presents normal mental development, no trisomy 21 manifestations; on the contrary, she had a few monosomy 21-like stigmata. She gave birth to a severely malformed infant with a pattern of malformations suggesting a partial 21-monosomy syndrome, but with a 46,XY normal karyotype in his peripheral blood lymphocytes. The findings are explained in the following way: the infant probably had originally a 47,XY,+21q- karyotype like his mother. Post zygotic nondisjunctional events produced a prevalent 46,XY,21q- line responsible for the severe malformations and the normal 46,XY line found in his blood lymphocytes.

Diseases presenting "severe malformations" symptom

  • congenital toxoplasmosis
  • megacystis-microcolon-intestinal hypoperistalsis syndrome
  • monosomy 21

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