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2. Optic nerve hypoplasia secondary to intracranial teratoma. Lee JT; Hall TR; Bateman JB Am J Ophthalmol; 1997 Nov; 124(5):705-6. PubMed ID: 9372735 [TBL] [Abstract][Full Text] [Related]
3. Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome: A case report. Shi H; Yang J; Guo Q; Zhang M Medicine (Baltimore); 2021 Mar; 100(10):e24991. PubMed ID: 33725872 [TBL] [Abstract][Full Text] [Related]
4. Ocular manifestations of Apert and Crouzon syndromes: qualitative and quantitative findings. Kreiborg S; Cohen MM J Craniofac Surg; 2010 Sep; 21(5):1354-7. PubMed ID: 20856021 [TBL] [Abstract][Full Text] [Related]
5. A newborn with acanthosis nigricans: can it be Crouzon syndrome with acanthosis nigricans? Sharda S; Panigrahi I; Gupta K; Singhi S; Kumar R Pediatr Dermatol; 2010; 27(1):43-7. PubMed ID: 20199409 [TBL] [Abstract][Full Text] [Related]
6. The spheno-occipital synchondrosis fuses prematurely in patients with Crouzon syndrome and midface hypoplasia compared with age- and gender-matched controls. Tahiri Y; Paliga JT; Vossough A; Bartlett SP; Taylor JA J Oral Maxillofac Surg; 2014 Jun; 72(6):1173-9. PubMed ID: 24480760 [TBL] [Abstract][Full Text] [Related]
7. Unilateral clinical anophthalmia with optic nerve hypoplasia in the fellow eye. Ceyhan D; See RF; Schnall BM J Pediatr Ophthalmol Strabismus; 2006; 43(2):116-8. PubMed ID: 16598982 [TBL] [Abstract][Full Text] [Related]
10. Correlation between Papilledema and Intracranial Hypertension in Crouzon Syndrome: A Case Report and Review of the Literature. Simonin A; Maduri R; Viaroli E; Levivier M; Daniel RT; Messerer M Pediatr Neurosurg; 2019; 54(4):223-227. PubMed ID: 31269504 [TBL] [Abstract][Full Text] [Related]
11. Optic canal characteristics in pediatric syndromic craniosynostosis. Hariri F; Farhana NA; Abdullah NA; Ibrahim N; Ramli NM; Mohd Abdullah AA; May CM; Khaliddin N J Craniomaxillofac Surg; 2021 Dec; 49(12):1175-1181. PubMed ID: 34247917 [TBL] [Abstract][Full Text] [Related]
13. Airway obstruction in the Crouzon syndrome: case report and review of the literature. Sirotnak J; Brodsky L; Pizzuto M Int J Pediatr Otorhinolaryngol; 1995 Mar; 31(2-3):235-46. PubMed ID: 7782181 [TBL] [Abstract][Full Text] [Related]
14. Completely cartilaginous trachea in a child with Crouzon syndrome. Devine P; Bhan I; Feingold M; Leonidas JC; Wolpert SM Am J Dis Child; 1984 Jan; 138(1):40-3. PubMed ID: 6546324 [TBL] [Abstract][Full Text] [Related]
15. Crouzon syndrome: association with absent pulmonary valve syndrome and severe tracheobronchomalacia. Beck R; Sertie AL; Brik R; Shinawi M Pediatr Pulmonol; 2002 Dec; 34(6):478-81. PubMed ID: 12422346 [TBL] [Abstract][Full Text] [Related]
16. [Acanthosis nigricans in children and Crouzon syndrome]. Lagaude M; Barreau M; Jokic M; Gerard M; DiRocco F; Hadj-Rabia S; Dompmartin A; Verneuil L Ann Dermatol Venereol; 2014 Nov; 141(11):685-8. PubMed ID: 25442473 [TBL] [Abstract][Full Text] [Related]
17. Optic nerve hypoplasia associated with chromosome 9 inversion. Cheung RT; Wong AM Can J Ophthalmol; 2009 Oct; 44(5):610-1. PubMed ID: 19789607 [No Abstract] [Full Text] [Related]
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20. Cephalometric analysis of hard and soft tissues in a 12-year-old syndromic child: a case report and update on dentofacial features of Crouzon syndrome. Nagaraju K; Ranadheer E; Suresh P; Tarun SP J Indian Soc Pedod Prev Dent; 2011; 29(4):315-9. PubMed ID: 22016316 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]