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dc.contributor.authorAk, G
dc.contributor.authorOzturk, S
dc.contributor.authorKurklu, E
dc.contributor.authorKoray, M
dc.contributor.authorTanyeri, H
dc.contributor.authorPalanduz, S
dc.date.accessioned2021-03-03T11:10:36Z
dc.date.available2021-03-03T11:10:36Z
dc.date.issued2005
dc.identifier.citationTanyeri H., Kurklu E., Ak G., Ozturk S., Koray M., Palanduz S., "Maxillofacial and dental manifestations in a patient with mandibulo-acral dysplasia", CRANIO-THE JOURNAL OF CRANIOMANDIBULAR PRACTICE, cilt.23, sa.1, ss.74-78, 2005
dc.identifier.issn0886-9634
dc.identifier.othervv_1032021
dc.identifier.otherav_2668054a-5884-4123-b9c7-3ab3fc7a144f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/30708
dc.identifier.urihttps://doi.org/10.1179/crn.2005.011
dc.description.abstractMandibulo-acral dysplasia (MAD) is a rare condition characterized by mandibular hypoplasia, acroosteolysis, delayed cranial suture closure, hypoplastic clavicles, stiff joints, dental crowding, atrophy of the skin of the hands and feet, progeroid facial appearance, alopecia and short stature. This report presents a patient with MAD, suffering from difficulty in mastication and speech, together with limited lip closure and aesthetic problems related to the clinical outcomes of the syndrome. The aim of reporting this case is to detail the first widely determined dental and maxillofacial abnormalities of a rare syndrome, mandibulo-acral dysplasia, and to contribute to the data regarding the etiology of consanguinity.
dc.language.isoeng
dc.subjectTıp
dc.subjectDiş Hekimliği
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectDİŞ HEKİMLİĞİ, ORAL CERRAHİ VE TIP
dc.titleMaxillofacial and dental manifestations in a patient with mandibulo-acral dysplasia
dc.typeMakale
dc.relation.journalCRANIO-THE JOURNAL OF CRANIOMANDIBULAR PRACTICE
dc.contributor.department, ,
dc.identifier.volume23
dc.identifier.issue1
dc.identifier.startpage74
dc.identifier.endpage78
dc.contributor.firstauthorID10973


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