Kjer ’ s disease associated with hypoacusis and late clinical manifestation

نویسنده

  • Yoshifumi Yamane
چکیده

A neuropatia óptica de Kjer, ou atrofia óptica dominante, é a mais frequente das neuropatias ópticas familiares. Trata-se de uma atrofia óptica de caráter autossômico dominante que se dá por uma alteração no gene OPA1, no cromossomo 3q28, com penetrância de 98% Apenas 15% dos casos possuem acuidade visual de 0,1 ou pior, apresentando ainda diferentes graus de atrofia do disco. Este relato objetiva descrever as características genéticas e clínicas da doença, bem como apresentar medidas de aconselhamento familiar. Para isso, será relatado um caso clínico de atrofia óptica dominante no qual se constata perda acentuada da acuidade visual, início de manifestações atipicamente tardias e hipoacusia bilateral. Descritores: Atrofia óptica autossômica dominante/genética; Surdez; Defeitos da visão cromática; Aconselhamento genético; Relatos de caso ABSTRACT

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Nekam’s Disease with Clinical Manifestation Simulating Darier's Disease: A Case Report

Nekam's disease is a rare dermatosis characterized by a distinctive seborrheic dermatitis with prominent facial eruption.  It is further associated with violaceous, papular, and/or nodular lesions on the extremities and trunk, typically arranged in a linear and reticulate pattern.  Herein, describe a patient with Nekam's disease, which resembled Darier’s disease in clinical manifestation.  The ...

متن کامل

Calcifying epithelial odontogenic (Pindborg) tumor involving a 16-year-old girl with no ‎prominent clinical manifestation: A case report

BACKGROUND AND AIM: The calcifying epithelial odontogenic tumor (CEOT) is a rare entity described by Pindborg and represents < 1% of all odontogenic tumors. Nearly 200 cases of this neoplasm have been reported to date. It mostly occurs in the posterior mandible associated with an impacted tooth, most often a mandibular molar. Patients are usually between 30 and 50 years of age, with no sex pred...

متن کامل

Psychiatric onset Alexander disease: an important challenge in neuropsychiatric diagnosis

Introduction: Alexander disease is a heterogenous group of diseases with various manifestations based on age of disease onset. This rare leukodystrophy syndrome with mutations in GFAP Gene could present with developmental delay and seizure in infantile form to ataxia and bulbar palsy in adulthood. However psychiatric symptoms are not well-defined and usually evaluate after disease diagnosis not...

متن کامل

The unusual presentation of genital Crohn’s disease in a patient with breast cancer: A case report

Cutaneous Crohn’s disease (CCD) is a relatively rare disease. Two-thirds of the affected patients are female with a mean age of onset of 35 years. CCD is divided into a genital type and an extra-genital type, each with their own unique different clinical manifestations. The usual presentation of genital Crohn’s disease (CD) is in the form of erythema and edema of the labia and scrotum. Here, we...

متن کامل

Causes of pediatric heart disease in Rasht and its relationship with clinical ‎manifestation and demographic characteristic

Introduction: Heart disease is the fifth cause of death in infants and children and &lrm;&rlm;%90&rlm;&lrm; of &lrm;these causes are related to congenital heart diseases.Nearly&rlm;%20&rlm;&lrm; of these children experience &lrm;heart failure and surgery, but life expectancy for these children is increased by palliative and &lrm;corrective surgeries. Demographic characteristics and clinical sym...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2014