Arhiva autor

Ioana Opriţoiu

Latest posts by Ioana Opriţoiu (see all)

Articole semnate de acelasi autor in Revista Romana de Pediatrie:

Solitary median maxillary central incisor syndrome – case report

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

Solitary median maxillary central incisor syndrome – case report

, , , and

ABSTRACT

Solitary median maxillary central incisor syndrome is a complex disorder consisting of multiple defects of development, mainly midline defects, secondary to the action of unknown factors operating in utero about the 35th-38th days from conception. The authors present a case of the child V.C. of 13 years and 9 months old, with repeated admissions for the assessment of short stature and mental retardation. At the age of 5 years the child was diagnosed with asthma, and at 10 years old with panhypopituitarism, and took inconstantly a thyroid replacement and growth hormone therapy. Clinical examination: severe short stature, facial dysmorphism, chronic nasal obstruction, the presence of a solitary median central incisor, moderate mental retardation with attention deficit. Laboratory examinations: cranial CT – pituitary hypoplasia; the hormonal tests confirmed the diagnosis of panhypopituitarism.

Key words: solitary median maxillary incisor syndrome, child

Full text | PDF

SINDROMUL INCISIVULUI MAXILAR MEDIAN UNIC

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

SINDROMUL INCISIVULUI MAXILAR MEDIAN UNIC

, , , and

REZUMAT

Sindromul incisivului maxilar median unic este o afecţiune complexă, datorată unor defecte multiple de dezvoltare, în special pe linia mediană, secundar acţiunii unor factori necunoscuţi, care acţionează în zilele 35-38 de viaţă intrauterină. Autorii prezintă cazul copilului V.C. în vârstă de 13 ani 9 luni, cu repetate internări în vederea evaluării pentru hipostatură şi retard mental. La vârsta de 5 ani a fost diagnosticat cu astm bronşic, iar la vârsta de 10 ani cu panhipopituitarism; a urmat tratament de substituţie tiroidiană şi cu hormon de creştere, dar inconstant. Examenul clinic: retard statural marcat, facies dismorf, obstrucţie nazală cronică, prezenţa incisivului maxilar median unic, retard mental moderat, cu deficit de atenţie. Examinări paraclinice: CT cranian – hipoplazie hipofizară, determinările hormonale au confirmat diagnosticul de panhipopituitarism.

Cuvinte cheie: sindromul incisivului maxilar median unic, copil

Full text | PDF