Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/15347
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dc.contributor.authorMarina Krstevska-Konstantinovaen_US
dc.contributor.authorKonstandina Kuzevska-Manevaen_US
dc.contributor.authorHristijan Nestoroven_US
dc.contributor.authorDaniela Georgievaen_US
dc.date.accessioned2021-11-08T13:56:50Z-
dc.date.available2021-11-08T13:56:50Z-
dc.date.issued2021-06-30-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/15347-
dc.description.abstractPoland syndrome (PS) is a rare congenital malformation, most commonly characterized by absence of chest wall muscles on one side of the body. It may be accompanied with other deformities of the extremities. We present the case of a 10-year-old girl with Poland syndrome and hypertrichosis of the back of the trunk and extremities. The clinical examination did not reveal the etiology of the syndrome, such as familial predisposition or some event that led to interrupted blood flow during the early embionic growth. The pregnancy was concieved with in vitro fertilization (IVF); triplets were born and our patient is one of these three girls. The hypertrychosis appeared at 8 years of life, without evidence of previous familial occurance, medications or hormonal disbalance. Other malformations that were found were: a mild form of kyphoscoliosis and mitral valve prolapse. The child was evaluated using a multidisciplinary approach, with further follow-up planned with surgical correction of the chest wall and breast augmentation.en_US
dc.language.isoenen_US
dc.publisherInstitute of Public Health of the Republic of North Macedonia = Институт за јавно здравје на Република Северна Македонијаen_US
dc.relation.ispartofArchives of Public Health = Архиви на јавното здравјеen_US
dc.subjectPoland syndromeen_US
dc.subjecthypertrichosisen_US
dc.subjectpubertyen_US
dc.subjectgirlen_US
dc.titleASSOCIATION OF POLAND SYNDROME AND HYPERTRICHOSIS IN A PUBERTAL GIRL - Case reporten_US
dc.typeArticleen_US
dc.identifier.doi10.3889/aph.2021.6003-
dc.identifier.urlhttps://www.id-press.eu/aph/article/view/6003/5500-
item.fulltextNo Fulltext-
item.grantfulltextnone-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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