Disorder of sexual development in a Holstein Friesian calf: Clinical, genetic, MRI and pathological findings

Abstract A 25‐day‐old Holstein Friesian singleton calf was presented with ambiguous external genitalia suggestive of a disorder of sexual development (DSD). Clinical examination revealed an abnormally positioned urogenital orifice caudal to the mammary complexes, with a palpable tubular structure resembling a hypoplastic penis. At 3 months of age, ultrasonography and magnetic resonance imaging identified bilateral ovaries with small follicles, uterine horns, a uterine body, cervix and a subcutaneous tubular structure of uncertain origin extending towards the perineal region. Endocrine evaluation at 6 months showed low testosterone (<25 pg/mL) and progesterone concentrations of 0.1–0.4 ng/mL during one oestrous cycle. Cytogenetic analysis revealed a normal female karyotype (60, XX) with a concurrent Robertsonian translocation, rob(1;29). Postmortem examination at 7 months confirmed a normal female reproductive tract, with the vagina narrowing into a tubular structure extending to the perineal region. The rob(1;29) translocation was considered unlikely to be causative, and the aetiology of the DSD remained undetermined.

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Publication Details

Journal
Veterinary Record Case Reports
Published
2026-11-01
DOI
https://doi.org/10.1002/vrc2.70679
Primary Topic
Sexual Differentiation and Disorders
Type
article
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article

Disorder of sexual development in a Holstein Friesian calf: Clinical, genetic, MRI and pathological findings

Erik A. W. S. Weerts, Stefanie Veraa, Peter R. Hut, J.M. Parlevliet et al.
Veterinary Record Case Reports
Sexual Differentiation and Disorders
article

Disorder of sexual development in a Holstein Friesian calf: Clinical, genetic, MRI and pathological findings

Erik A. W. S. Weerts, Stefanie Veraa, Peter R. Hut, J.M. Parlevliet, Janice S. M. van der Laan
article en

Abstract

Abstract A 25‐day‐old Holstein Friesian singleton calf was presented with ambiguous external genitalia suggestive of a disorder of sexual development (DSD). Clinical examination revealed an abnormally positioned urogenital orifice caudal to the mammary complexes, with a palpable tubular structure resembling a hypoplastic penis. At 3 months of age, ultrasonography and magnetic resonance imaging identified bilateral ovaries with small follicles, uterine horns, a uterine body, cervix and a subcutaneous tubular structure of uncertain origin extending towards the perineal region. Endocrine evaluation at 6 months showed low testosterone (<25 pg/mL) and progesterone concentrations of 0.1–0.4 ng/mL during one oestrous cycle. Cytogenetic analysis revealed a normal female karyotype (60, XX) with a concurrent Robertsonian translocation, rob(1;29). Postmortem examination at 7 months confirmed a normal female reproductive tract, with the vagina narrowing into a tubular structure extending to the perineal region. The rob(1;29) translocation was considered unlikely to be causative, and the aetiology of the DSD remained undetermined.

Veterinary Record Case ReportsVol. 14(4)
Utrecht University (NL)
Openalex Percentile: Top 22%
Sexual Differentiation and Disorders
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