CASE REPORT KALLMANN SYNDROME IN A 14-YEAR-OLD BOY

  • Melisa Anggraeni
  • Made Arimbawa
  • IW Bikin Suryawan

Abstract

Kallmann syndrome is a combination of hypogonadotropic–hypogonadism due to gonadotropine releasing hormone (GnRH) deficiency with anosmia or hyposmia. Magnetic resonance imaging (MRI) reveals hypoplasia or aplasia of the olfactory bulbs. The incidence is estimated at 1 in 10.000 and 50.000 males and females respectively. The main clinical features consists of the absence of spontaneous puberty, partial or total loss of the sense of smell (anosmia). In this case report, we describe a 14 year old boy with Kallmann syndrome who was refferred with delayed puberty and lack of smell function. Physical examination revealed Tanner stage I and proven anosmia from olfactory test. Laboratory test showed low titer of testosteron. Testicular ultrasonography (USG) revealed small testicles. Treatment of this particular patient was with a 25 mg of intramuscular testosterone injection and were then increased by 25 mg every two weeks. Proper management of patients with Kallmann syndrome usually allows them to attain normal reproductive health.

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Author Biographies

Melisa Anggraeni

Department of Child Health, Medical School,

Udayana University, Sanglah Hospital, Denpasar, Bali

Made Arimbawa

Department of Child Health, Medical School,

Udayana University, Sanglah Hospital, Denpasar, Bali

IW Bikin Suryawan

Department of Child Health, Medical School,

Udayana University, Sanglah Hospital, Denpasar, Bali

How to Cite
ANGGRAENI, Melisa; ARIMBAWA, Made; SURYAWAN, IW Bikin. CASE REPORT KALLMANN SYNDROME IN A 14-YEAR-OLD BOY. Medicina, [S.l.], v. 44, n. 1, oct. 2013. ISSN 2540-8321. Available at: <https://ojs.unud.ac.id/index.php/medicina/article/view/6840>. Date accessed: 21 nov. 2024.
Section
Articles

Keywords

Kallmann syndrome, hypogonadotropic-hypogonadism, anosmia

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