168 related articles for article (PubMed ID: 32523159)
1. Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome.
Knežević P; Tarle M; Fratrić LI; Tarle A; Knežević-Krajina H; Macan D
Acta Stomatol Croat; 2020 Mar; 54(1):69-74. PubMed ID: 32523159
[TBL] [Abstract][Full Text] [Related]
2. Multisystemic Manifestations of Hyaline Fibromatosis Syndrome: Implications for Diagnosis and Management.
Albusta N; Isa HM; Al-Jowder HE
Cureus; 2023 Oct; 15(10):e47250. PubMed ID: 37859675
[TBL] [Abstract][Full Text] [Related]
3. Hyaline Fibromatosis Syndrome: A Rare Inherited Disorder.
Mantri MD; Pradeep MM; Kalpesh PO; Pranavsinh RJ
Indian J Dermatol; 2016; 61(5):580. PubMed ID: 27688461
[TBL] [Abstract][Full Text] [Related]
4. Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.
Casas-Alba D; Martínez-Monseny A; Pino-Ramírez RM; Alsina L; Castejón E; Navarro-Vilarrubí S; Pérez-Dueñas B; Serrano M; Palau F; García-Alix A
Hum Mutat; 2018 Dec; 39(12):1752-1763. PubMed ID: 30176098
[TBL] [Abstract][Full Text] [Related]
5. Hyaline fibromatosis syndrome: a case presenting with gingival enlargement as the only clinical manifestation and a report of two new mutations in the ANTXR2 gene.
Liu Y; Zeng X; Ding Y; Xu Y; Duan D
BMC Oral Health; 2021 Oct; 21(1):508. PubMed ID: 34627224
[TBL] [Abstract][Full Text] [Related]
6. Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome.
Daşar T; Gönen HN; Kösemehmetoğlu K; Tekşam Ö; Boduroğlu K; Utine GE; Şimşek Kiper PÖ
Turk J Pediatr; 2024 May; 66(2):205-214. PubMed ID: 38814306
[TBL] [Abstract][Full Text] [Related]
7. Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review.
Zhu Y; Du X; Sun L; Wang H; Wang D; Wu B
Mol Genet Genomic Med; 2022 Aug; 10(8):e1993. PubMed ID: 35726349
[TBL] [Abstract][Full Text] [Related]
8. A Severe Case of Infantile Systemic Hyalinosis in an Asian Child: A Product of Consanguinity.
Baroud S; Alawadhi A
Cureus; 2021 Jul; 13(7):e16433. PubMed ID: 34414050
[TBL] [Abstract][Full Text] [Related]
9. Protein-losing enteropathy and joint contractures caused by a novel homozygous ANTXR2 mutation.
Schussler E; Linkner RV; Levitt J; Mehta L; Martignetti JA; Oishi K
Adv Genomics Genet; 2018; 8():17-21. PubMed ID: 30050362
[TBL] [Abstract][Full Text] [Related]
10. Infantile Systemic Hyalinosis: A Case Report and Literature Review.
Mohammed SE; Mohammed MM; Saeed M; Al Zahrani D; Alasmari BG
Cureus; 2023 Oct; 15(10):e46519. PubMed ID: 37927741
[TBL] [Abstract][Full Text] [Related]
11. Clinical aspects of Hyaline Fibromatosis Syndrome and identification of a novel mutation.
Härter B; Benedicenti F; Karall D; Lausch E; Schweigmann G; Stanzial F; Superti-Furga A; Scholl-Bürgi S
Mol Genet Genomic Med; 2020 Jun; 8(6):e1203. PubMed ID: 32196989
[TBL] [Abstract][Full Text] [Related]
12. Infantile systemic hyalinosis: a case report with a novel mutation.
Al Sinani S; Al Murshedy F; Abdwani R
Oman Med J; 2013 Jan; 28(1):53-5. PubMed ID: 23386947
[TBL] [Abstract][Full Text] [Related]
13. Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report.
Jaouad IC; Guaoua S; Hajjioui A; Sefiani A
J Med Case Rep; 2014 Sep; 8():291. PubMed ID: 25186005
[TBL] [Abstract][Full Text] [Related]
14. Treatment of Massive Labial and Gingival Hypertrophy in a Patient With Infantile Systemic Hyalinosis-A Case Report.
Krasuska-Sławińska E; Polnik D; Rokicki D; Koeber B
J Oral Maxillofac Surg; 2015 Oct; 73(10):1962.e1-5. PubMed ID: 26207694
[TBL] [Abstract][Full Text] [Related]
15. Hyaline Fibromatosis Syndrome: Early Outcomes Following Major Craniofacial Mass Excision.
Chaisrisawadisuk S; Rattana-Arpa S; Vathanophas V; Sathienkijkanchai A
J Craniofac Surg; 2024 Jun; ():. PubMed ID: 38847516
[TBL] [Abstract][Full Text] [Related]
16. A novel splice site mutation in ANTXR2 (CMG2) gene results in systemic hyalinosis.
Wang YY; Wen CQ; Wei Z; Jin X
J Pediatr Hematol Oncol; 2011 Dec; 33(8):e355-7. PubMed ID: 22042284
[TBL] [Abstract][Full Text] [Related]
17. Hyaline fibromatosis syndrome: A rare case of multifocal intra-articular involvement.
DeVita R; Faraji N; Nakfoor R; Elliott R; Kosmas C
Clin Imaging; 2021 Feb; 70():51-55. PubMed ID: 33120290
[TBL] [Abstract][Full Text] [Related]
18. Hyaline Fibromatosis Syndrome Diagnosed by Whole Genome Sequencing.
Anderson S
J Pediatr Health Care; 2024 Feb; ():. PubMed ID: 38385928
[TBL] [Abstract][Full Text] [Related]
19. Overlapping Hyaline Fibromatosis Syndrome: A Rare Case of Juvenile Hyaline Fibromatosis and Infantile Systemic Hyalinosis.
Oswal RM; Prasad SS; Manohar N; Pise GA; Rao K
Cureus; 2022 Aug; 14(8):e27947. PubMed ID: 36120216
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]