For: | Ge XY, Ge L, Hu WW, Li XL, Hu YY. Growth hormone therapy for children with KBG syndrome: A case report and review of literature. World J Clin Cases 2020; 8(6): 1172-1179 [PMID: 32258089 DOI: 10.12998/wjcc.v8.i6.1172] |
---|---|
URL: | https://www.wjgnet.com/2307-8960/full/v8/i6/1172.htm |
Number | Citing Articles |
1 |
Dongye He, Mei Zhang, Yanying Li, Fupeng Liu, Bo Ban. Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database search. Orphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03301-y
|
2 |
Badiginchala Naga Jyothi, Sumathi Angel, Chinthalapalli Prakash Ravi Kumar, Parag M Tamhankar. Child with KBG syndrome. BMJ Case Reports 2024; 17(12): e260238 doi: 10.1136/bcr-2024-260238
|
3 |
Enise Avci Durmusalioglu, Esra Isik, Turkan Turkut Tan, Yusuf Can Dogan, Banu Nur, Burcu Yeter, Aslihan Sanri, Dilek Uludag Alkaya, Serife Ozturk Yilmaz, Akcahan Akalin, Gizem Urel Demir, Aysegul Yilmaz, Merve Sogukpinar, Oznur Yilmaz Bayer, Ozlem Giray Bozkaya, Ozlem Sezer, Pelin Ozlem Simsek Kiper, Gulen Eda Utine, Beyhan Tuysuz, Ozgur Cogulu, Ercan Mihci, Tahir Atik. Genotypic and Phenotypic Landscape of KBG Syndrome: A Study of 23 Turkish Individuals. American Journal of Medical Genetics Part A 2025; doi: 10.1002/ajmg.a.64128
|
4 |
Yunha Choi, Jungmin Choi, Hyosang Do, Soojin Hwang, Go Hun Seo, In Hee Choi, Changwon Keum, Jin‐Ho Choi, Minji Kang, Gu‐Hwan Kim, Han‐Wook Yoo, Beom Hee Lee. KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature. Molecular Genetics & Genomic Medicine 2023; 11(4) doi: 10.1002/mgg3.2127
|
5 |
Davide Mattei, Paolo Cavarzere, Rossella Gaudino, Franco Antoniazzi, Giorgio Piacentini. DYSMORPHIC features and adult short stature: possible clinical markers of KBG syndrome. Italian Journal of Pediatrics 2021; 47(1) doi: 10.1186/s13052-021-00961-5
|
6 |
Stephanie Ho, Ho‐Ming Luk, Ivan F. M. Lo. KBG syndrome in a Chinese population: A case series. American Journal of Medical Genetics Part A 2022; 188(6): 1693 doi: 10.1002/ajmg.a.62688
|
7 |
Marie Adamo-Croux, Adriane Auger-Gilli, Gwenaël Le Guyader, Juliette Aubin-Courjault, Henri Margot, Claire Bar, Didier Lacombe, Julien Van-Gils, Marine Legendre, Aurélien Binet, Xavier Le Guillou Horn. Care pathways in childhood neurodevelopmental disorders: Toward greater awareness of KBG syndrome among pediatricians. Archives de Pédiatrie 2024; 31(5): 320 doi: 10.1016/j.arcped.2024.02.007
|
8 |
Su Jin Kim, Aram Yang, Ji Sun Park, Dae Gyu Kwon, Jeong-Seop Lee, Young Se Kwon, Ji Eun Lee. Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review. Frontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.579805
|
9 |
Fenqi Gao, Xiu Zhao, Bingyan Cao, Xin Fan, Xiaoqiao Li, Lele Li, Shengbin Sui, Zhe Su, Chunxiu Gong. Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature. Journal of Personalized Medicine 2022; 12(3): 407 doi: 10.3390/jpm12030407
|