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BMC Pediatr ; 23(1): 506, 2023 10 13.
Artigo em Inglês | MEDLINE | ID: mdl-37828451

RESUMO

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.


Assuntos
Anormalidades Múltiplas , Anormalidades Craniofaciais , Fibromatose Gengival , Síndrome da Fibromatose Hialina , Humanos , Feminino , Lactente , Fibromatose Gengival/diagnóstico , Fibromatose Gengival/genética , Fibromatose Gengival/patologia , Anormalidades Múltiplas/genética , Anormalidades Craniofaciais/diagnóstico
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