Disease: Gingival fibromatosis facial dysmorphism
- 'Splitting versus lumping': Temple-Baraitser and Zimmermann-Laband Syndromes
- A case of Zimmermann-Laband syndrome with supernumerary teeth
- A Japanese Boy with Dysmorphic Syndrome with Multiple Pituitary Hormone Deficiency and Gingival Fibromatosis Due to a Pathogenic KCNQ1 Variant
- A rare case of gingival fibromatosis associated with hypertrichosis and a dysmorphic face
- A recurrent KCNK4 variant in a dominant pedigree with hypertrichosis and gingival fibromatosis syndrome: Variable phenotypic expressivity and insights on patients' dental management
- Aggressive fibromatosis in the jaw and facial region with bone involvement. A review
- Ambras syndrome: A rare case report
- Arthropathy, osteolysis, keloids, relapsing conjunctival pannus and gingival overgrowth: a variant of polyfibromatosis?
- Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres
- Autosomal recessive gingival fibromatosis with distinctive facies
- Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants
- Clinical and genetic study of two patients with Zimmermann-Laband syndrome and literature review
- Congenital marked hypertrichosis and Laband syndrome in a child: overlap between the gingival fibromatosis-hypertrichosis and Laband syndromes
- De Novo 17q24.2-q24.3 microdeletion presenting with generalized hypertrichosis terminalis, gingival fibromatous hyperplasia, and distinctive facial features
- Delineating the 17q24.2-q24.3 microdeletion syndrome phenotype
- Enamel renal syndrome: A case report with calcifications in pulp, gingivae, dental follicle and kidneys
- Epilepsy in KCNH1-related syndromes
- Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome
- Familial cherubism: the experience of the Moscow Central Institute for Stomatology and Maxillo-Facial Surgery
- Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca<sup>2+</sup>-Activated K<sup>+</sup> Channel SK3 Cause Zimmermann-Laband Syndrome
- Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes
- Gingival enlargement: Practical management
- Gingival fibromatosis associated with cherubism
- Gingival fibromatosis combined with cherubism and psychomotor retardation: a rare syndrome
- Gingival fibromatosis with prune-belly syndrome
- Gingival fibromatosis, short stature, border-line IQ, facial dysmorphism and hepatomegaly
- Gingival proteomics reveals the role of TGF beta and YAP/TAZ signaling in Raine syndrome fibrosis
- Hereditary gingival fibromatosis in a family with the Zimmermann-Laband syndrome
- Hereditary gingival fibromatosis with distinctive facies
- Hereditary gingival fibromatosis: a case report
- HEREDITARY GINGIVAL FIBROMATOSIS. REPORT OF AN AFFECTED FAMILY WITH ASSOCIATED SPLENOMEGALY AND SKELETAL AND SOFT-TISSUE ABNORMALITIES
- Hypertrichosis universalis congenita: a separate entity, or the same disease as gingival fibromatosis?
- Infantile systemic hyalinosis
- Juvenile hyalin fibromatosis
- Juvenile hyaline fibromatosis
- Juvenile hyaline fibromatosis
- Juvenile hyaline fibromatosis (JHF)
- Juvenile hyaline fibromatosis (Murray-Puretic-Drescher syndrome): oral and systemic findings in siblings
- Juvenile hyaline fibromatosis: clinical heterogeneity in three patients
- Juvenile hyaline fibromatosis: report of a case and comparison with infantile systemic hyalinosis
- Juvenile hyaline fibromatosis: two new patients and review of the literature
- Laband syndrome: a case report
- Laband syndrome. Report of two cases, review of the literature, and identification of additional manifestations
- Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
- Oral fibromas and fibrosis. The clinical picture, histology and differential diagnosis
- Pseudo-sarcomatous fibromatosis. An exceptional case with buccal localization
- Pseudomalignancies in dermatology
- Stomatologic alterations in childhood, part III
- Syndromes with gingival fibromatosis: A systematic review
- Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K<sup>+</sup> channelopathies
- Syndromic gingival fibromatosis
- The Robinow syndrome: an isolated case with a detailed study of the phenotype
- Wide clinical spectrum in Zimmermann-Laband syndrome
- Zimmermann-Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions
- Zimmermann-Laband syndrome in a patient with severe mental retardation
- Zimmermann-Laband syndrome in an adult. Long-term follow-up of a patient with vascular and cardiac complications
- Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant
- Zimmermann-Laband syndrome with bilateral developmental cataract - a new association?