Nance–Horan syndrome
| Nance–Horan syndrome | |
|---|---|
| Other names | X-linked congenital cataracts and microcornea, X-linked cataract–dental syndrome, cataracts-oto-dental syndrome, cataract–dental syndrome, and mesiodens–cataract syndrome. |
 | |
| This condition is inherited in an X-linked dominant manner. | |
| Specialty | Ophthalmology |
Nance–Horan syndrome, also known as X-linked congenital cataracts and microcornea, X-linked cataract–dental syndrome, cataracts-oto-dental syndrome, cataract–dental syndrome, and mesiodens–cataract syndrome, is a rare X-linked syndrome characterized by eye and teeth abnormalities, intellectual disability, and facial deformities.[1][2]
Signs and symptoms
[edit]The main ocular sign of Nance–Horan syndrome is a congenital nuclear cataract which results in reduced visual acuity. Other ocular features include microphthalmia, microcornea, strabismus, and nystagmus. Dental features include tapered premolar/molar cusps, supernumerary teeth, screwdriver-shaped incisors, and diastema. Abnormal facial features include anteverted pinnae, prominent and bulbous nose, and long narrow face. 30% of males with Nance–Horan syndrome have intellectual disabilities. Carrier females exhibit less severe clinical symptoms, including lens opacities at the posterior Y-sutures with minimal or no loss of vision, modest face dysmorphism, and dental abnormalities.[2]
Genetics
[edit]This syndrome is caused by mutations in the Nance Horan gene (NHS) which is located on the short arm of the X chromosome (Xp22.13).[3]
Diagnosis
[edit]![[icon]](/wiki/File:Wiki_letter_w_cropped.svg){kind=small} | This section is empty. You can help by adding to it. (August 2017) |
Management
[edit]There is no known cure for this syndrome. Patients usually need ophthalmic surgery and may also need dental surgery. Genetic counseling and screening of the mother's relatives is recommended.[citation needed]
History
[edit]This syndrome was first described by Margaret B. Horan and Walter Elmore Nance in 1974.[4][5]
References
[edit]- ^ De Souza, Neil; Chalakkal, Paul; Martires, Sergio; Soares, Renita (2019). "Oral manifestations of Nance–Horan syndrome: A report of a rare case". Contemporary Clinical Dentistry. 10 (1): 174–177. doi:10.4103/ccd.ccd_490_18. ISSN 0976-237X. PMC 6975004. PMID 32015664.
- ^ a b Guven, Yeliz; Saracoglu, Hilal Piril; Aksakal, Sermin Dicle; Kalayci, Tugba; Altunoglu, Umut; Uyguner, Zehra Oya; Eraslan, Serpil; Borklu, Esra; Kayserili, Hulya (2023-05-23). "Nance-Horan Syndrome: characterization of dental, clinical and molecular features in three new families". BMC Oral Health. 23 (1): 314. doi:10.1186/s12903-023-03029-4. ISSN 1472-6831. PMC 10204325. PMID 37221585.
- ^ Tug, Esra; Dilek, Nihal F.; Javadiyan, Shahrbanou; Burdon, Kathryn P.; Percin, Ferda E. (2013). "A Turkish family with Nance-Horan syndrome due to a novel mutation". Gene. 525 (1): 141–145. doi:10.1016/j.gene.2013.03.094. PMID 23566852.
- ^ Horan, Margaret B.; Billson, F. A. (1974). "X-Linked Cataract and Hutchinsonian Teeth". Journal of Paediatrics and Child Health. 10 (2): 98–102. doi:10.1111/j.1440-1754.1974.tb01098.x. S2CID 71936293.
- ^ Nance, WE; Warburg, M; Bixler, D; Helveston, EM (1974). "Congenital X-linked cataract, dental anomalies and brachymetacarpalia". Birth Defects Original Article Series. 10 (4): 285–91. PMID 4470901.
Further reading
[edit]- Li, Huajin; Yang, Lizhu; Sun, Zixi; Yuan, Zhisheng; Wu, Shijing; Sui, Ruifang (2018-02-05). "A novel small deletion in the NHS gene associated with Nance-Horan syndrome". Scientific Reports. 8 (1). Springer Science and Business Media LLC. doi:10.1038/s41598-018-20787-2. ISSN 2045-2322. PMC 5799206.
- Yu, Xuelin; Zhao, Yueyue; Yang, Zhenghua; Chen, Xing; Kang, Gangjing (2024). "Genetic research on Nance-Horan syndrome caused by a novel mutation in the NHS gene". Gene. 906. Elsevier BV: 148223. doi:10.1016/j.gene.2024.148223. ISSN 0378-1119. PMID 38286268.
External links
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