A 7-month-old boy with breathing problems.

نویسنده

  • Robert Listernick
چکیده

برای دانلود رایگان 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

Unusual Presentation of Splenogonadal Fusion in a 7-Month-Old Male Infant

Introduction: Splenogonadal fusion is a rare congenital anomaly characterized with anomalous fusion of the spleen and the gonad or mesonephric derivatives. Herein, we report the case of a 7-month-old boy with unusual presentation of splenogonadal fusion. Case Presentation</...

متن کامل

Starburst crystals in urine.

A 7-month-old boy was brought to the emergency department for persistent cough and difficulty in breathing. On the second day of admission, his urine was analyzed to rule out urinary tract infection. Chemical analysis of the sample was unremarkable and sediment microscopy did not show any abnormalities except for dense dark crystals (Fig. 1). Individual crystals were needle shaped, while aggreg...

متن کامل

Esophageal Foreign Body: A Case Report of a Refractory Croup in a 20-Month-Old Boy

Introduction: Foreign body ingestion is common among children and more common in boys and in children under the age of 3. It can present with a wide variety of symptoms like dysphagia and drooling or symptoms related to the upper aerodigestive tract.   Case Report: A 20-month-old male presented with refractory croup and poor feeding since 2 weeks. Bronchoscopy and esophagoscopy was performed du...

متن کامل

Bloody nipple discharge in a 7-month-old boy.

Isolated bloody nipple discharge is rare in infancy and is usually idiopathic. Discharge commonly resolves spontaneously, and ultrasonography is a useful diagnostic technique to detect the cause of discharge. The authors report a 7-month-old boy who presented with unilateral spontaneous bloody nipple discharge for 1 month without signs of infection or mass.

متن کامل

Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutation.

The authors report the unusual clinical and neurophysiologic features of a sporadic case of a boy carrying an 806delG mutation on the MECP2 gene. A 28-month-old boy was examined for severe developmental delay, seizures, microcephaly, breathing dysfunction, and spontaneous and evoked myoclonic jerks of upper limbs. Neurophysiologic study proved the cortical origin of myoclonus; however, it was n...

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

عنوان ژورنال:
  • Pediatric annals

دوره 40 1  شماره 

صفحات  -

تاریخ انتشار 2011