Van Wyk–Grumbach Syndrome: A Rare Manifestation of Juvenile Hypothyroidism

Background Van Wyk–Grumbach (VWG) syndrome is a rare complication of juvenile hypothyroidism characterized by precocious puberty, delayed bone age, and ovarian cysts. Case presentation We report the case of an 8-year-old girl who presented with intermittent vaginal bleeding and abdominal pain. Imaging revealed bilateral multiseptate ovarian cystic lesions. She had been advised to undergo surgical management at a community health center and was subsequently referred to our institution. Following comprehensive clinical, radiological, and biochemical evaluation, a diagnosis of VWG syndrome was established. Conclusion VWG syndrome should be considered in pediatric females with bilateral ovarian enlargement and precocious puberty, particularly in the context of delayed bone age and hypothyroidism. Prompt thyroid hormone replacement can prevent unnecessary surgical procedures.

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Publication Details

Journal
Indian journal of clinical medicine
Published
2026-03-11
DOI
https://doi.org/10.1177/26339447261428785
Primary Topic
Genetic Syndromes and Imprinting
Type
article
Field-Weighted Citation Impact
0.00
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article

Van Wyk–Grumbach Syndrome: A Rare Manifestation of Juvenile Hypothyroidism

Madhuri Pundlikrao Udgire, Varun Vasant Nimje
Indian journal of clinical medicine
Genetic Syndromes and Imprinting
article

Van Wyk–Grumbach Syndrome: A Rare Manifestation of Juvenile Hypothyroidism

Madhuri Pundlikrao Udgire, Varun Vasant Nimje
article en

Abstract

Background Van Wyk–Grumbach (VWG) syndrome is a rare complication of juvenile hypothyroidism characterized by precocious puberty, delayed bone age, and ovarian cysts. Case presentation We report the case of an 8-year-old girl who presented with intermittent vaginal bleeding and abdominal pain. Imaging revealed bilateral multiseptate ovarian cystic lesions. She had been advised to undergo surgical management at a community health center and was subsequently referred to our institution. Following comprehensive clinical, radiological, and biochemical evaluation, a diagnosis of VWG syndrome was established. Conclusion VWG syndrome should be considered in pediatric females with bilateral ovarian enlargement and precocious puberty, particularly in the context of delayed bone age and hypothyroidism. Prompt thyroid hormone replacement can prevent unnecessary surgical procedures.

Indian journal of clinical medicine
Government of Maharashtra (IN), Government Medical College (IN), Government Medical College (IN)
Good health and well-being
Openalex Percentile: Top 26%
Genetic Syndromes and Imprinting
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