Sindrome di Cook
Contenuto principale dell'articolo
Abstract
La sindrome di Cook è una malattia rara con una costellazione di caratteristiche a causa del coinvolgimento sistemico. Qui descriviamo un caso di sindrome di Cook associata a cataratta.
Downloads
Dettagli dell'articolo

Questo lavoro è fornito con la licenza Creative Commons Attribuzione - Non commerciale 4.0 Internazionale.
Riferimenti bibliografici
Cooks RG, Hertz M, Katznelson MBM., Goodman RM. A new nail dysplasia syndrome with onychonychia and absence and/or hypoplasia of distal phalanges. Clinical genetics 1985; 27(1): 85-91.
Chatterjee D. Congenital anonychia and brachydactyly of the left foot – Cooks syndrome variant: Case report and review of literature. Indian J Hum Genet 2014; 20: 206-8.
Brennan CB, Buehler T, Lesher JL Jr. Cooks syndrome: A case report and brief review. Pediatr Dermatol 2013;30:e52-3.
Genzer-Nir M, Khayat M, Kogan L, Cohen HI, Hershkowitz M, Geiger D, et al. Mammary- digital- nail (MDN) syndrome; European Journal of human Genetics 2010;18(6): 662-667.
Patel BK, Vasava RR, Rathod MB, Singh VP. Rare case report “Cooks syndrome, Mammary Digit Nail syndrome(MDN)”.INDIAN JOURNAL OF APPLIED RESEARCH 2014;4(6):356-57.
Shashikumar BM, Harish MR, Bhadbhade SP, Deepadarshan K. Cooks syndrome. Indian J Paediatr Dermatol 2015;16:93-5.
Rishana N, Narasimhan M, Ramakrishnan R, Abdullah AK. Congenital absence of the nails: A variant of Cooks syndrome. Indian J Paediatr Dermatol 2024;25:308-10.