Van Wyk–Grumbach syndrome: Decoding the mystery of precocious puberty with delayed bone age

ABSTRACT A 5-year 7-month-old girl was brought by her mother due to an inability to gain height for 3.5 years, associated with facial puffiness, dry and coarse skin, and constipation for the past 3 years. Physical examination revealed stigmata of hypothyroidism along with bilateral breast enlargement. Investigations showed elevated thyroid-stimulating hormone levels, elevated prolactin levels, elevated anti-thyroid peroxidase antibody levels, low luteinizing hormone levels, bilateral ovarian cysts on ultrasound, and delayed bone age. She was diagnosed with disproportionate severe short stature and gonadotropin-independent isosexual precocity, that is, Van Wyk–Grumbach syndrome due to autoimmune hypothyroidism.

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Publication Details

Journal
IJEM Case Reports
Published
2025-10-01
DOI
https://doi.org/10.4103/ijemcr.ijemcr_23_25
Primary Topic
Congenital limb and hand anomalies
Type
article
Field-Weighted Citation Impact
0.00
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article

Van Wyk–Grumbach syndrome: Decoding the mystery of precocious puberty with delayed bone age

Pawan Kumar Goel, Anshul Tiwari, Lakhan Singh
IJEM Case Reports
Congenital limb and hand anomalies
article

Van Wyk–Grumbach syndrome: Decoding the mystery of precocious puberty with delayed bone age

Pawan Kumar Goel, Anshul Tiwari, Lakhan Singh
article en

Abstract

ABSTRACT A 5-year 7-month-old girl was brought by her mother due to an inability to gain height for 3.5 years, associated with facial puffiness, dry and coarse skin, and constipation for the past 3 years. Physical examination revealed stigmata of hypothyroidism along with bilateral breast enlargement. Investigations showed elevated thyroid-stimulating hormone levels, elevated prolactin levels, elevated anti-thyroid peroxidase antibody levels, low luteinizing hormone levels, bilateral ovarian cysts on ultrasound, and delayed bone age. She was diagnosed with disproportionate severe short stature and gonadotropin-independent isosexual precocity, that is, Van Wyk–Grumbach syndrome due to autoimmune hypothyroidism.

IJEM Case ReportsVol. 3(4)
Lala Lajpat Rai Memorial Medical College (IN)
Openalex Percentile: Top 61%
Congenital limb and hand anomalies
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