منابع مشابه
Dyskeratosis Congenita: A Report of Two Cases
Oral manifestations play an important role in the diagnosis of many systemic conditions. Dyskeratosis congenita (DC) is a rare genodermatosis which exhibits oral leukoplakia, nail dystrophy, and reticular skin pigmentations as its primary features. DC has increased risk of developing constitutional anemias and malignancies and early diagnosis enables the patient to be monitored and proper inter...
متن کاملDyskeratosis congenita: report of two cases with distinct clinical presentations.
Dyskeratosis congenita (DC) is a rare, inheritable disorder characterized by a triad of abnormal skin pigmentation, nail dystrophy and mucosal leukoplakia. Inheritance is mainly X-linked recessive; however, autosomal dominant and recessive forms have also been reported. Here, we report two cases of DC with distinct clinical presentations together with different genetic screening results, which ...
متن کاملReport of Two Cases of Zinsser-Cole- Engman (Dyskeratosis Congenita) Syndrome- A Rare Entity
ZinsserCole-Engman syndrome, also known as dyskeratosis congenita, is a rare genetic disorder characterized by triad of pigmentation and atrophy of the skin, leukokeratoses of oral mucosa and nail dystrophy along with bone marrow failure and predisposition to cancer [1]. The condition can be inherited as autosomal recessive, autosomal dominant and rarely X linked. It is proposed that mutations ...
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ژورنال
عنوان ژورنال: Orthopedics & Traumatology
سال: 1959
ISSN: 1349-4333,0037-1033
DOI: 10.5035/nishiseisai.9.17