دورية أكاديمية
Zimmermann-Laband syndrome and infantile systemic hyalinosis: an enigma with two separate terms with overlapping features: a case report.
| العنوان: | Zimmermann-Laband syndrome and infantile systemic hyalinosis: an enigma with two separate terms with overlapping features: a case report. |
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| المؤلفون: | Owlia F; Department of Oral and Maxillofacial Medicine, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran., Navabazam A; Department of Oral and Maxillofacial Surgery, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran., Akhavan-Karbasi MH; Department of Oral and Maxillofacial Medicine, School of Dentistry, Yazd Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran., Derakhshan Barjoei MM; Dentistry student, Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. mmdb1378@gmail.com.; USERN Office, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. mmdb1378@gmail.com. |
| المصدر: | BMC pediatrics [BMC Pediatr] 2023 Oct 13; Vol. 23 (1), pp. 506. Date of Electronic Publication: 2023 Oct 13. |
| نوع المنشور: | Case Reports; Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: BioMed Central Country of Publication: England NLM ID: 100967804 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2431 (Electronic) Linking ISSN: 14712431 NLM ISO Abbreviation: BMC Pediatr Subsets: MEDLINE |
| أسماء مطبوعة: | Original Publication: London : BioMed Central, [2001- |
| مواضيع طبية MeSH: | Hyaline Fibromatosis Syndrome* , Fibromatosis, Gingival*/diagnosis , Fibromatosis, Gingival*/genetics , Fibromatosis, Gingival*/pathology , Abnormalities, Multiple*/genetics , Craniofacial Abnormalities*/diagnosis, Humans ; Female ; Infant |
| مستخلص: | Background: Zimmermann-Laband Syndrome (ZLS) and infantile systemic hyalinosis (ISH) are rare genetic disorders. They are characterized by various spectrum manifestations. In spite of other case reports, this case with features of both syndromes was reported by oral medicine specialists and oral and maxillofacial surgeons. Case Presentation: In this study, we reported an 18-months old female patient with gingival overgrowth. This phenomenon completely embedded all the erupted teeth. In this case, the presence of multiple papulonodular cutaneous lesions is a newly observed aspect that has rarely been reported in the existing literature. Gingival overgrowth was excised under general anesthesia. At six months of follow-up after surgery, mastication and breathing problems were improved. Aesthetic aspects were ameliorated in terms of gingival appearance. Conclusions: To date, due to the ambiguous presentations, both syndromes remain an enigma for specialists. A timely diagnosis could be crucial for prognosis and preventing severe further surcharge. Dentists could play an important role in the diagnosis of rare disorders. (© 2023. BioMed Central Ltd., part of Springer Nature.) |
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| فهرسة مساهمة: | Keywords: Case report; Gingival enlargement; Infantile systemic hyalinosis; Papulonodular lesions; Zimmermann-Laband Syndrome |
| SCR Disease Name: | Zimmerman Laband syndrome |
| تواريخ الأحداث: | Date Created: 20231012 Date Completed: 20231023 Latest Revision: 20231213 |
| رمز التحديث: | 20231215 |
| مُعرف محوري في PubMed: | PMC10571462 |
| DOI: | 10.1186/s12887-023-04344-z |
| PMID: | 37828451 |
| قاعدة البيانات: | MEDLINE |
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Full Text Finder | تدمد: | 1471-2431 |
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| DOI: | 10.1186/s12887-023-04344-z |