139 related articles for article (PubMed ID: 32428224)
1. Kenny-Caffey syndrome type 2.
Yerawar C; Kabde A; Deokar P
QJM; 2021 Jul; 114(4):267-269. PubMed ID: 32428224
[No Abstract] [Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Oral rehabilitation of a patient with Kenny-Caffey syndrome using telescopic overdenture.
Nazar A; George R; Mathew N
J Indian Prosthodont Soc; 2021; 21(2):204-207. PubMed ID: 33938872
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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]
15. Dwarfism and cortical thickening of tubular bones. Transient hypocalcemia in a mother and son.
Kenny FM; Linarelli L
Am J Dis Child; 1966 Feb; 111(2):201-7. PubMed ID: 5322798
[No Abstract] [Full Text] [Related]
16. Pseudopapilledema in Kenny-Caffey syndrome.
Beral L; Donnio A; Jean-Charles A; Merle H
J Pediatr Ophthalmol Strabismus; 2011; 48 Online():e1-3. PubMed ID: 19791716
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Unusual cause of hypocalcemic seizures in a neonate.
Dewan P; Gidaganti S; Faridi MM; Batra P; Sudhanshu S
Indian J Pediatr; 2014 Aug; 81(8):831-2. PubMed ID: 24297340
[No Abstract] [Full Text] [Related]
19. A case of infantile cortical hyperostosis; Caffey-Smyth syndrome.
THOMPSON CG
Conn State Med J; 1949 Jan; 13(1):28. PubMed ID: 18103328
[No Abstract] [Full Text] [Related]
20. Conference on infantile cortical hyperostoses (Caffey-Smyth syndrome).
BURKE FG
J Pediatr; 1948 Apr; 32(4):441-8. PubMed ID: 18908820
[No Abstract] [Full Text] [Related]
[Next] [New Search]
