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E. Boia

Latest posts by E. Boia (see all)

  • KALLMANN Syndrome – case report - 03/08/2015
  • SINDROM KALLMANN - 03/08/2015

Articole semnate de acelasi autor in Revista Romana de Pediatrie:

KALLMANN Syndrome – case report

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Revista Romana de PEDIATRIE | Volumul LX, Nr. 3, An 2011
ISSN 1454-0398  |  e-ISSN 2069-6175
ISSN-L 1454-0398
DOI: 10.37897/RJP

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KALLMANN Syndrome – case report

I. Velea, Corina Paul, Ionela Tămăşan, Loredana Todorescu-Negru, E. Boia, F. Bîrsăşteanu and D. Oneţ

ABSTRACT

Kallmann Syndrome is classically characterized by isolated GnRH deficit associated with hypo/anosmia. Clinically the patients presented micropenis, cryptorchidism, absence of puberty occurence, infertility. The paper presents the case of an adolescent aged 16, presenting anosmia and hypogonadism (observed by family) even since he was 3 years old. He was evaluated repeatedly in different medical services, but no clear diagnosis was made. Finally, the patient was admitted in Clinic II Pediatrics for investigations and diagnosis.

Key words: anosmia, hypogonadism, testosteron

Full text | PDF

I. Velea

SINDROM KALLMANN

SELECT ISSUE

Revista Romana de PEDIATRIE | Volumul LX, Nr. 3, An 2011
ISSN 1454-0398  |  e-ISSN 2069-6175
ISSN-L 1454-0398
DOI: 10.37897/RJP

Indexed

DOI - Crossref
Similarity Check by iThenticate, worldwide No 1 professional plagiarism checking system
DOAJ
Ebsco Host - Medline
Google Academic
Semantic Scholar

HIGHLIGHTS

ICMJE- Recommendations

Read the Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly work in Medical Journals.

Promoting Global Health

The published medical research literature is a global public good. Medical journal editors have a social responsibility to promote global health by publishing, whenever possible, research that furthers health worldwide.

Partners

Partners

SINDROM KALLMANN

I. Velea, Corina Paul, Ionela Tămăşan, Loredana Todorescu-Negru, E. Boia, F. Bîrsăşteanu and D. Oneţ

REZUMAT

Sindromul Kallmann se caracterizează prin deficit izolat de GnRH, asociat cu hipo/anosmie. La examenul clinic al pacienţilor cu sindrom Kallmann se decelează micropenis, criptorhidie, absenţa instalării pubertăţii, infertilitate. Se prezintă cazul unui adolescent în vârstă de 16 ani, afirmativ cu anosmie şi hipogonadism (sesizat de aparţinători) încă de la vârsta de 2-3 ani. A fost evaluat în repetate rânduri în diferite servicii medicale, fără a se stabili un diagnostic de certitudine. Ulterior, pacientul se internează în Clinica II Pediatrie pentru investigaţii suplimentare şi precizare de diagnostic.

Cuvinte cheie: anosmie, hipogonadism, testosteron

Full text | PDF

I. Velea


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