2026-10-19T00:29:25Zhttps://ebyu-rdlopen.rawdatalibrary.net/oai/request

oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/167862026-10-18T20:38:54Zopenairedrivercom_ebyu_10000col_ebyu_10001

A case of weill-marchesani syndrome with a novel mutation and vitamin d deficiencyYildirim, Malik EjderVural, AyseKurtulgan, Hande KucukKilicgun, HasanBaser, BurakWeill-Marchesani SyndromeMicrospherophakiaGlaucomaBrachydactylyVitamin D DeficiencyMedicine, General & InternalGeneral & Internal MedicineWeill-Marchesani syndrome is an inherited connective tissue disorder. It is characterized by various ocular abnormalities and some skeletal problems. It is rarely seen in the world, but the clinical complications are significant and may require some interventions such as eye surgery, physical therapy or orthopedic procedures. Here we report on an eleven year old female with glaucoma, ectopia lentis, microspherophakia, brachydactyly and vitamin D deficiency from Sivas, Turkey. She was suffering from Weill-Marchesani syndrome with ADAMTS10 mutation.DERMAN MEDICAL PUBL2018Articlehttps://rdlopen.rawdatalibrary.net/r/ebyu/16786https://doi.org/10.4328/jcam.57181309-0720enJOURNAL OF CLINICAL AND ANALYTICAL MEDICINEinfo:eu-repo/semantics/openAccessinfo:eu-repo/semantics/articlehttps://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/16786