Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma : More Than a Random Association?

المؤلفون المشاركون

Longinotti, Maurizio
Cottoni, Francesca
Poddie, Fausto
Cucca, Francesco
Galleu, Antonio
Contini, Salvatore
Fozza, Claudio

المصدر

Case Reports in Hematology

العدد

المجلد 2011، العدد 2011 (31 ديسمبر/كانون الأول 2011)، ص ص. 1-3، 3ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2011-08-10

دولة النشر

مصر

عدد الصفحات

3

التخصصات الرئيسية

الأمراض

الملخص EN

Keratitis-ichthyosis-deafness (KID) syndrome is a rare congenital disorder characterized by skin lesions, neurosensorial hypoacusia, and keratitis, usually due to the c.148G→A mutation involving the connexin 26 gene.

We report on a KID patient who showed the atypical c.101T→C mutation and developed a T-cell lymphoma so far never described in this group of patients.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Fozza, Claudio& Poddie, Fausto& Contini, Salvatore& Galleu, Antonio& Cottoni, Francesca& Longinotti, Maurizio…[et al.]. 2011. Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma : More Than a Random Association?. Case Reports in Hematology،Vol. 2011, no. 2011, pp.1-3.
https://search.emarefa.net/detail/BIM-503042

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Fozza, Claudio…[et al.]. Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma : More Than a Random Association?. Case Reports in Hematology No. 2011 (2011), pp.1-3.
https://search.emarefa.net/detail/BIM-503042

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Fozza, Claudio& Poddie, Fausto& Contini, Salvatore& Galleu, Antonio& Cottoni, Francesca& Longinotti, Maurizio…[et al.]. Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma : More Than a Random Association?. Case Reports in Hematology. 2011. Vol. 2011, no. 2011, pp.1-3.
https://search.emarefa.net/detail/BIM-503042

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-503042