ArticleJournal of reproduction & infertility
A Case of Primary Hypogonadism with Features of Albright's Syndrome.
Article in Journal of reproduction & infertility. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed, 2 citations in OpenAlex.
- Case Report: Bilateral congenital fourth metacarpal shortening in a competitive softball athlete with preserved function.Frontiers in surgery · 2026Article
- Application of two-dimensional and three-dimensional ultrasound in prenatal screening for brachydactyly deformity.American journal of translational research · 2020Article
- Unilateral shortening of third metacarpal bone in a patient with tuberous sclerosis.European journal of rheumatology · 2019Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundMcCune Albright syndrome is rare with an estimated prevalence of 1 in 100,000 to 1 in 1,000,000 persons. The classical clinical triad consists of fibrous dysplasia of the bone, café-au-lait skin spots and precocious puberty. However, in rare cases, there may be primary hypogonadism and amenorrhea. CASE PRESENTATION: An eighteen-year-old female presented with amenorrhea. She had a short stature, round face, thick neck, and short fourth metacarpals and metatarsals. The secondary sexual characters were absent. Serum calcium, phosphorus and parathyroid concentrations were normal, but gonadotropin hormones were very low. X-ray examination revealed short fourth and fifth metacarpals, short left metatarsal, and short fibula.
conclusionThese local bony abnormalities along with the biochemical findings helped us to diagnose this case as an unusual presentation of primary hypogonadism with features of McCune Albright's syndrome where there was amenorrhea rather than preocious puberty.
Indexed as
Identifiers
27478774PMC4947208W2421932574What OpenQuestion holds
Registered trials
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