Zimmermann-Laband syndrome: Clinical and cytogenetic study in two related patients | Zendy

Sadegh Shirian | Zendy; Hasan Shahabinejad | Zendy; Abolfazl Saeedzadeh | Zendy; Khosrow Daneshbod | Zendy; Hengameh Khosropanah | Zendy; Mojtaba Mortazavi | Zendy; Yahya Daneshbod | Zendy

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Zimmermann-Laband syndrome: Clinical and cytogenetic study in two related patients

Author(s) -

Sadegh Shirian,

Hasan Shahabinejad,

Abolfazl Saeedzadeh,

Khosrow Daneshbod,

Hengameh Khosropanah,

Mojtaba Mortazavi,

Yahya Daneshbod

Publication year - 2019

Publication title -

journal of clinical and experimental dentistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.481

H-Index - 23

ISSN - 1989-5488

DOI - 10.4317/jced.55214

Subject(s) - biology , genome browser , genetics , comparative genomic hybridization , genome , gene duplication , human genetics , chromosome , copy number variation , computational biology , gene , genomics

Zimmermann-Laband Syndrome (ZLS) is an extremely rare autosomal dominant congenital disorder. It is a craniofacial malformation syndrome with predominant intraoral involvement consisting of gingival fibromatosis diffusion in early development. The molecular basis of ZLS is still unknown. Although familial aggregation with different inheritance patterns is detected in ZLS patients, most of the cases are sporadic.

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