Sindrome di Cook

Contenuto principale dell'articolo

Anubhav Chauhan
Dr. Tanuja
Deepak Kumar Sharma

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.

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Dettagli dell'articolo

Come citare
[1]
Chauhan, A., Tanuja, D. e Sharma, D.K. 2025. Sindrome di Cook. Italian Journal of Prevention, Diagnostic and Therapeutic Medicine. 8, 2 (giu. 2025), 116-118. DOI:https://doi.org/10.30459/2025-27.
Sezione
Case report

Riferimenti bibliografici

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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.

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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.