A novel report of a fertile female with partial Y chromosome gain completing a healthy pregnancy

Author:

Coleman John1ORCID,Kavanagh Karl1,Kesterton Ian2,Hegarty Ann‐Marie3,O'Connell Susan M.45,Lynch Sally Ann16

Affiliation:

1. Department of Clinical Genetics Children's Health Ireland at Crumlin Crumlin Ireland

2. Department of Cytogenetics, Viapath Guy's Hospital London UK

3. Department of Cytogenetics Children's Health Ireland at Crumlin Crumlin Ireland

4. Department of Endocrinology Children's Health Ireland at Crumlin Crumlin Ireland

5. Department of Paediatrics Royal College of Surgeons Ireland Dublin Ireland

6. School of Medicine University College Dublin Dublin Ireland

Abstract

AbstractWe present a female patient with a complex sex chromosomal rearrangement [GRCh38] Xp22.33(10701_981101)x1,Yq11.221q11.23(13948013_26483746)x1 who conceived spontaneously and carried a healthy pregnancy to term. The patient presented with extreme short stature (more than 4SD below expected) and a bilateral Madelung deformity suggesting a possible SHOX deletion. The patient was otherwise medically well. This patient's short stature was found to be a result of a complex chromosome rearrangement involving a partial X chromosome deletion, which included the SHOX gene and a gain of Y chromosomal material. The Y chromosome material did not contain the SRY gene locus. This is the first recorded case to date of this rearrangement in a female who spontaneously conceived which resulted in a live birth. This patient had normal external and internal anatomy and normal endocrine evaluation with normal puberty. X‐inactivation studies revealed no evidence of skewed inactivation.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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