128 related articles for article (PubMed ID: 3893111)
1. Unusual cause of short stature.
Larsen JL; Kivlin J; Odell WD
Am J Med; 1985 Jun; 78(6 Pt 1):1025-32. PubMed ID: 3893111
[TBL] [Abstract][Full Text] [Related]
2. The Kenny-Caffey syndrome: growth retardation and hypocalcemia in a young boy.
Lee WK; Vargas A; Barnes J; Root AW
Am J Med Genet; 1983 Apr; 14(4):773-82. PubMed ID: 6342392
[TBL] [Abstract][Full Text] [Related]
3. Adult Chinese twins with Kenny-Caffey syndrome type 2: A potential age-dependent phenotype and review of literature.
Cheng SSW; Chan PKJ; Luk HM; Mok MT; Lo IFM
Am J Med Genet A; 2021 Feb; 185(2):636-646. PubMed ID: 33263187
[TBL] [Abstract][Full Text] [Related]
4. Further delineation of phenotype and genotype of Kenny-Caffey syndrome type 2 (phenotype and genotype of KCS type 2).
Chen X; Zou C
Mol Genet Genomic Med; 2024 Apr; 12(4):e2433. PubMed ID: 38591167
[TBL] [Abstract][Full Text] [Related]
5. [Kenny-Caffey syndrome and its related syndromes].
Isojima T; Kitanaka S
Nihon Rinsho; 2015 Nov; 73(11):1959-64. PubMed ID: 26619675
[TBL] [Abstract][Full Text] [Related]
6. Characterization of optical coherence topography findings in Kenny-Caffey syndrome.
Timoney P; Darcy F; McCreery K; Reardon W; Brosnahan D
J AAPOS; 2007 Jun; 11(3):291-3. PubMed ID: 17360206
[TBL] [Abstract][Full Text] [Related]
7. Mother and daughter with Kenny-Caffey syndrome: the adult phenotype.
Tonelli L; Sanchini M; Margutti A; Buldrini B; Superti-Furga A; Ferlini A; Selvatici R; Bigoni S
Eur J Med Genet; 2024 Jun; 69():104943. PubMed ID: 38679371
[TBL] [Abstract][Full Text] [Related]
8. A recurrent de novo FAM111A mutation causes Kenny-Caffey syndrome type 2.
Isojima T; Doi K; Mitsui J; Oda Y; Tokuhiro E; Yasoda A; Yorifuji T; Horikawa R; Yoshimura J; Ishiura H; Morishita S; Tsuji S; Kitanaka S
J Bone Miner Res; 2014 Apr; 29(4):992-8. PubMed ID: 23996431
[TBL] [Abstract][Full Text] [Related]
9. The Kenny syndrome, a rare type of growth deficiency with tubular stenosis, transient hypoparathyroidism and anomalies of refraction.
Majewski F; Rosendahl W; Ranke M; Nolte K
Eur J Pediatr; 1981 Mar; 136(1):21-30. PubMed ID: 7215388
[TBL] [Abstract][Full Text] [Related]
10. Case report: Late middle-aged features of
Ohmachi Y; Urai S; Bando H; Yokoi J; Yamamoto M; Kanie K; Motomura Y; Tsujimoto Y; Sasaki Y; Oi Y; Yamamoto N; Suzuki M; Shichi H; Iguchi G; Uehara N; Fukuoka H; Ogawa W
Front Endocrinol (Lausanne); 2022; 13():1073173. PubMed ID: 36686468
[TBL] [Abstract][Full Text] [Related]
11. Kenny-Caffey Syndrome Type 2: A Unique Presentation and Craniofacial Analysis.
Turner AE; Abu-Ghname A; Davis MJ; Shih L; Volk AS; Streff H; Buchanan EP
J Craniofac Surg; 2020; 31(5):e471-e475. PubMed ID: 32310878
[TBL] [Abstract][Full Text] [Related]
12. Ocular findings in Kenny's syndrome.
Boynton JR; Pheasant TR; Johnson BL; Levin DB; Streeten BW
Arch Ophthalmol; 1979 May; 97(5):896-900. PubMed ID: 444124
[TBL] [Abstract][Full Text] [Related]
13. [Arabian variant of Kenny syndrome: a familial case in Tunisia].
Fitouri Z; Fayech C; Ferchichi M; Ben Becher S
Ann Endocrinol (Paris); 2005 Sep; 66(4):361-4. PubMed ID: 16392187
[TBL] [Abstract][Full Text] [Related]
14. Overlapping phenotype comprising Kenny-Caffey type 2 and Sanjad-Sakati syndromes: The first case report.
Cavole TR; Perrone E; de Faria Soares MF; Dias da Silva MR; Maeda SS; Lazaretti-Castro M; Alvarez Perez AB
Am J Med Genet A; 2020 Dec; 182(12):3029-3034. PubMed ID: 33010201
[TBL] [Abstract][Full Text] [Related]
15. FAM111A mutations result in hypoparathyroidism and impaired skeletal development.
Unger S; Górna MW; Le Béchec A; Do Vale-Pereira S; Bedeschi MF; Geiberger S; Grigelioniene G; Horemuzova E; Lalatta F; Lausch E; Magnani C; Nampoothiri S; Nishimura G; Petrella D; Rojas-Ringeling F; Utsunomiya A; Zabel B; Pradervand S; Harshman K; Campos-Xavier B; Bonafé L; Superti-Furga G; Stevenson B; Superti-Furga A
Am J Hum Genet; 2013 Jun; 92(6):990-5. PubMed ID: 23684011
[TBL] [Abstract][Full Text] [Related]
16. Kenny syndrome: evidence for idiopathic hypoparathyroidism in two patients and for abnormal parathyroid hormone in one.
Fanconi S; Fischer JA; Wieland P; Atares M; Fanconi A; Giedion A; Prader A
J Pediatr; 1986 Sep; 109(3):469-75. PubMed ID: 3746537
[TBL] [Abstract][Full Text] [Related]
17. Kenny-Caffey syndrome in two sibs born to consanguineous parents: evidence for an autosomal recessive variant.
Franceschini P; Testa A; Bogetti G; Girardo E; Guala A; Lopez-Bell G; Buzio G; Ferrario E; Piccato E
Am J Med Genet; 1992 Jan; 42(1):112-6. PubMed ID: 1308349
[TBL] [Abstract][Full Text] [Related]
18. Oral manifestations of patients with Kenny-Caffey Syndrome.
Moussaid Y; Griffiths D; Richard B; Dieux A; Lemerrer M; Léger J; Lacombe D; Bailleul-Forestier I
Eur J Med Genet; 2012; 55(8-9):441-5. PubMed ID: 22522175
[TBL] [Abstract][Full Text] [Related]
19. Mother-to-daughter transmission of Kenny-Caffey syndrome associated with the recurrent, dominant FAM111A mutation p.Arg569His.
Nikkel SM; Ahmed A; Smith A; Marcadier J; Bulman DE; Boycott KM
Clin Genet; 2014 Oct; 86(4):394-5. PubMed ID: 24635597
[No Abstract] [Full Text] [Related]
20. Kenny-Caffey syndrome. Case report and literature review.
Abdel-Al YK; Auger LT; el-Gharbawy F
Clin Pediatr (Phila); 1989 Apr; 28(4):175-9. PubMed ID: 2649298
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
