טוען...
Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome
Hyaline fibromatosis syndrome (HFS) is a rare autosomal recessive genetic disorder characterized by accumulation of hyalinized fibrous tissue with cutaneous, mucosal, osteoarticular, and systemic involvement. The condition is caused by a mutation of ANTXR2 gene that results in a faulty synthesis of...
שמור ב:
| הוצא לאור ב: | Acta Stomatol Croat |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
University of Zagreb School of Dental Medicine, and Croatian Dental Society - Croatian Medical Association
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7233120/ https://ncbi.nlm.nih.gov/pubmed/32523159 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15644/asc54/1/8 |
| תגים: |
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