Multiple Exostosis and Embryonic Clubfoot in a Premature Newborn: Case Report
نویسندگان
چکیده
منابع مشابه
a case report of diaphragmatic eventration in a premature newborn
background diaphragm of eventration is a defect of whole or a part of diaphragm muscle and replacing it with fibroplastic tissue. the incidence of eventration is uncertain. the article aims to report a newborn with congenital diaphragmatic eventration. case report the case is a dysmorphic male premature newborn which born at 33 gestational age. due to sever respiratory distress the patient admi...
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Newborns’ bacterial infections due to group B Streptococcus (GBS) happen in two forms including early-onset disease or late-onset disease. In this paper, we report a case of early-onset GBS infection in a male infant. A 22-year-old primigravid woman delivers a term normal looking male infant. Nasal flaring, grunting, and poor feeding presented soon after birth. An empiric treatment wit...
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BACKGROUND Ganglioneuroblastoma is a tumor of peripheral neuroblastic tissue which occurs predominantly in the pediatric age group; it is a rare occurrence in the newborn period with only one case reported at birth to date. CASE PRESENTATION We report the case of a newborn male baby of Brahmin ethnicity from Nepal who presented with respiratory distress and blueberry muffin skin lesions after...
متن کاملSubacromial impingement syndrome in a patient with hereditary multiple exostosis: a case report
BACKGROUND Hereditary multiple exostosis (HME) is characterised by multiple osteochondromas that are distributed throughout the skeleton, invariably involving the shoulder girdle. Tumours within the subacromial space can cause secondary irritation of the rotator cuff and result in subacromial impingement syndrome. CASE PRESENTATION We describe a 19 year old female patient with HME who present...
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Osteochondroma of the spine is rare. It may present in solitary or multiple form (hereditary multiple exostoses). Herein, we report a case of an 18-year-old male who was diagnosed with thoracic osteochondroma, originating from the D4 vertebra with intraspinal extension and spinal cord compression in hereditary multiple exostosis. The patient was managed with surgery. Complete tumour excision wa...
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ژورنال
عنوان ژورنال: Archives in Neurology & Neuroscience
سال: 2020
ISSN: 2641-1911
DOI: 10.33552/ann.2020.08.000689