نتایج جستجو برای: clinical characteristic

تعداد نتایج: 1316807  

Journal: :Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 2018

Journal: :dental research journal 0
deepankar misra sapna panjwani shalu rai akansha misra mukul prabhat prashant gupta

background: to evaluate the efficacy of color doppler ultrasound (cdus) in differentiating benign and malignant cervical lymph nodes by detecting differences in blood flow patterns. materials and methods: in this cross‑sectional prospective study, 25 untreated patients with clinical evidence of cervical lymphadenopathy were evaluated. cdus was performed for 80 cervical lymph nodes. the gray sca...

N Adibi S Shamsadini S Zandi

Hutchinson-Gilford progeria syndrome is an extremely rare condition with features of premature and accelerated aging. The pattern of inheritance is unclear, although autosomal dominant mutations have been proposed. The disease presentation is usually in infancy and early childhood with a characteristic phenotype of short stature, abnormal skin and nail, beaked nose, loss of subcutaneous f...

Atousa Janeshin, Seyedeh Porousha Mahjoub Khatibani,

Hemifacial microsomia is a rare congenital malformation of craniofacial structures. Its characteristic features are unilateral underdevelopment of the face and ear malformations. This study describes clinical and radiographical features of a rare case of a 4-year-old hemifacial microsomia patient with underdevelopment of the left side of the face and preauricular skin tags on the affected side...

Farhad Malekzad Mehdi Qeisari Nastaran Namazi Zahra Asadi Kani

The association between actinic granuloma and giant cell arteritis (temporal arteritis) has been claimed by some authors. There is a hypothesis that actinic radiation has the principal role in the etiology of both diseases in a similar way. Here, we report a case of actinic granuloma that had characteristic pathologic features of giant cell arteritis in histopathologic examination without clini...

احسانی‌پور, فهیمه,

    Introduction: Cornelia de lange syndrome(CDLS) is a rare syndrome which is characterized by multiple congenital anomalies, mental retardation, characteristic facial appearance, developmental delay, skeletal malformation, hirsutism, and various ophthalmologic problems. The diagnosis of this syndrome is clinical. Case Report: The patient of the present case report was an infant with cornelia ...

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