These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
132 related articles for article (PubMed ID: 32128008)
1. Kleeblattschädel in Pfeiffer syndrome type II. Pfeifer CM Radiol Case Rep; 2020 May; 15(5):474-478. PubMed ID: 32128008 [TBL] [Abstract][Full Text] [Related]
2. Pfeiffer syndrome in an adult with previous surgical correction: A case report of CT findings. Duggal N; Omer A; Jupalli S; Pisinski L; Krauthamer AV Radiol Case Rep; 2021 Sep; 16(9):2463-2468. PubMed ID: 34257781 [TBL] [Abstract][Full Text] [Related]
3. Pfeiffer type 2 syndrome: review with updates on its genetics and molecular biology. Rai R; Iwanaga J; Dupont G; Oskouian RJ; Loukas M; Oakes WJ; Tubbs RS Childs Nerv Syst; 2019 Feb; ():. PubMed ID: 30740633 [TBL] [Abstract][Full Text] [Related]
6. Studies of malformation syndromes in man XXXVI: the Pfeiffer syndrome, association with Kleeblattschädel and multiple visceral anomalies. Case report and review. Hodach RJ; Viseskul C; Gilbert EF; Herrmann JP; Wolfson JJ; Kaveggia EG; Opitz JM Z Kinderheilkd; 1975; 119(2):87-103. PubMed ID: 1136537 [TBL] [Abstract][Full Text] [Related]
7. Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child. Soekarman D; Fryns JP; van den Berghe H Genet Couns; 1992; 3(4):217-20. PubMed ID: 1472357 [TBL] [Abstract][Full Text] [Related]
9. Ophthalmic considerations in patients with Pfeiffer syndrome. Clark JD; Compton CJ; Tahiri Y; Nunery WR; Harold Lee HB Am J Ophthalmol Case Rep; 2016 Jul; 2():1-3. PubMed ID: 29503887 [TBL] [Abstract][Full Text] [Related]
11. Pfeiffer Syndrome Type 3 and Prune Belly Anomaly in a Female: Case Report and Review. Peña-Padilla C; Viramontes-Aguilar L; Tavares-Macías G; Bobadilla-Morales L; L Cunningham M; Park S; Zapata-Aldana E; Corona-Rivera JR Fetal Pediatr Pathol; 2019 Oct; 38(5):412-417. PubMed ID: 31002276 [No Abstract] [Full Text] [Related]
12. Prenatal ultrasound diagnosis of a case of Pfeiffer syndrome without cloverleaf skull and review of the literature. Nazzaro A; Della Monica M; Lonardo F; Di Blasi A; Baffico M; Baldi M; Nazzaro G; De Placido G; Scarano G Prenat Diagn; 2004 Nov; 24(11):918-22. PubMed ID: 15565658 [TBL] [Abstract][Full Text] [Related]
13. Genetic Syndromes Associated with Craniosynostosis. Ko JM J Korean Neurosurg Soc; 2016 May; 59(3):187-91. PubMed ID: 27226847 [TBL] [Abstract][Full Text] [Related]
14. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis. Cohen MM Am J Med Genet; 1993 Feb; 45(3):300-7. PubMed ID: 8434615 [TBL] [Abstract][Full Text] [Related]
16. Pfeiffer Syndrome type 2--case report. Oyamada MK; Ferreira HS; Hoff M Sao Paulo Med J; 2003 Jul; 121(4):176-9. PubMed ID: 14595512 [TBL] [Abstract][Full Text] [Related]
17. Craniosynostosis and congenital tracheal anomalies in an infant with Pfeiffer syndrome carrying the W290C FGFR2 mutation. Chen CP; Lin SP; Su YN; Chien SC; Tsai FJ; Wang W Genet Couns; 2008; 19(2):165-72. PubMed ID: 18618990 [TBL] [Abstract][Full Text] [Related]