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1.
J Ayub Med Coll Abbottabad ; 34(4): 880-882, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36566420

RESUMEN

Acrodermatitis Enteropathica is a rare hereditary condition characterized by perioral dermatitis, diarrhoea, and alopecia. Aetiology includes autosomal recessive inheritance and acquired causes such as protein malnutrition, malabsorption syndromes, premature births, parenteral nutrition, chronic illnesses, and alcoholism. We report a rare case of a 12-year-old boy who presented with cutaneous manifestations involving the whole body, diarrhoea, and sparse hairs. A low level of plasma zinc, and alkaline phosphatase level was found, and he was started on zinc supplements. He significantly improved in a few days, and was discharged after counselling the parents about treatment compliance. This case highlights importance of early diagnosis, and the importance of treatment compliance in Acrodermatitis Enteropathica. It also stresses the need to take measures to ensure the provision of health facilities especially in remote areas.


Asunto(s)
Acrodermatitis , COVID-19 , Masculino , Humanos , Niño , COVID-19/complicaciones , Control de Enfermedades Transmisibles , Zinc/uso terapéutico , Acrodermatitis/diagnóstico , Acrodermatitis/etiología , Diarrea
2.
J Ayub Med Coll Abbottabad ; 34(4): 895-897, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36566424

RESUMEN

Ectodermal Dysplasia (ED) is a rare genetic condition characterized by the involvement of ectoderm derivatives such as hair, nail, sweat glands, and teeth. It has many variants, but the two most common ones are hypohidrotic/anhidrotic ectodermal dysplasia and hidrotic ectodermal dysplasia. Herein, we present a case of a 20-year-old female with hypohidrotic ectodermal dysplasia who had anodontia, hypohidrosis, and hypotrichosis, and her condition went unrecognized until she was seen for gastroenteritis at a tertiary care center. This case report will help spread education and awareness regarding such a rare and under-recognized condition. Early diagnosis and intervention help improve the quality of life.


Asunto(s)
Anodoncia , Displasia Ectodermal Anhidrótica Tipo 1 , Displasia Ectodérmica , Humanos , Femenino , Adulto Joven , Adulto , Displasia Ectodermal Anhidrótica Tipo 1/complicaciones , Displasia Ectodermal Anhidrótica Tipo 1/diagnóstico , Calidad de Vida , Displasia Ectodérmica/complicaciones , Displasia Ectodérmica/diagnóstico , Anodoncia/etiología
3.
BMJ Case Rep ; 15(11)2022 Nov 25.
Artículo en Inglés | MEDLINE | ID: mdl-36428031

RESUMEN

Dengue infection is common in 129 countries including Pakistan, with an estimated 390 million dengue virus infections per year. Asia accounts for 70% of the actual burden. Clinical signs and symptoms of dengue include a high fever (40°C/104 °F) accompanied by two of the following symptoms during the febrile phase: severe headache, pain behind the eyes, muscle and joint pains, nausea, vomiting, swollen glands and rash. Severe dengue is a potentially fatal complication, due to plasma leaking, fluid accumulation, respiratory distress, severe bleeding or organ impairment. Dengue virus does not usually cause neurological manifestations, unlike other arboviral infections. Encephalopathy is the most common neurological complication. Encephalitis is rare manifestation. We report a rare case of dengue encephalitis from Pakistan, with extensive brain lesions involving the thalamus, cerebellar vermis and frontoparietal periventricular regions. Therefore, we suggest dengue encephalitis should be considered in the differential diagnosis of fever with altered sensorium, especially in Asian countries such as Pakistan where dengue is rampant as dengue encephalitis can be fatal at times.


Asunto(s)
Virus del Dengue , Dengue , Encefalitis , Enfermedades del Sistema Nervioso , Humanos , Dengue/complicaciones , Dengue/diagnóstico , Pakistán , Encefalitis/complicaciones , Fiebre/complicaciones , Encéfalo/diagnóstico por imagen
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