scholarly journals Werdnig-Hoffmann Disease in A Female Child: A Rare Case Report

2016 ◽  
Author(s):  
Dr Tapan Kumar Biswas ◽  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Female Child ◽  
Rare Case Report ◽  
Werdnig Hoffmann

The fatal cholera like diarrhoea in coronavirus disease 2019(COVID-19)- a rare case report in toddler

2020 ◽  
Vol 11 (SPL1) ◽  
pp. 1894-1897
Author(s):  
Varsha Gajbhiye ◽  
Shubhangi Patil (Ganvir) ◽  
Sarika Gaikwad
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Digestive System ◽  
Gastrointestinal Symptoms ◽  
Female Child ◽  
Multiple Organ ◽  
Mild Case ◽  
Severe Dehydration ◽  
Rare Case Report ◽  
History Of

A 14-month female child came with complain of cholera like watery loose stool 10-12 times and vomiting 6-7 times, 24 hrs before admission. She was in severe dehydration, hypotension, unconscious with no recorded fever during her stay in hospital and no history of contact with COVID-19. Patient was COVID-19 positive Dehydration and hypotension was corrected, metabolic acidosis continued and eventually patient succumb due to multiple organ failure. This case report should arouse us to suspect COVID infection in every acute Gastroenteritis child who may not have any common symptoms as seen in COVID patient, also who have no history of significant contact with COVID positive patient in family. Some people with COVID-19 develop gastrointestinal symptoms either alone or with respiratory symptoms. Recently, researchers at Stanford University found that a third of patients they studied with a mild case of COVID-19 had symptoms affecting the digestive system. Another recent study Trusted Source published by researchers in Beijing found that anywhere from 3 to 79 percent of people with COVID-19 develop gastrointestinal symptoms.

A rare case report of autoimmune haemolytic anemia in a female child due to a Donath-Landsteiner antibody

2020 ◽  
Vol 27 (2) ◽  
pp. 83-86
Author(s):  
Z. Radonjić ◽  
B. Andrić ◽  
O. Šerbić ◽  
D. Mićić ◽  
M. Kuzmanović ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Female Child ◽  
Rare Case Report ◽  
Haemolytic Anemia

scholarly journals Kindler syndrome: A rare case report

2021 ◽  
Vol 2 (5) ◽  
Author(s):  
Apoorva D Chopkar ◽  
◽  
Sakshi S Malpani ◽  
Bhagyashree B Supekar ◽  
Jayesh I Mukhi ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Female Child ◽  
Kindler Syndrome ◽  
Infancy And Childhood ◽  
Rare Case Report ◽  
Cutaneous Atrophy

Kindler Syndrome (KS) is a rare hereditary disorder characterized by acral blistering of infancy and childhood, photosensitivity, progressive poikiloderma, and cutaneous atrophy. We report this case of KS in a 4 year old female child on account of its rarity Keywords: Kindler syndrome; acral blistering; pokiloderma; photosensitivity

Sinus histiocytosis and massive lymphadenopathy (Rosai-Dorfman disease) in an 8 year old female child: a rare case report

2015 ◽  
Vol 4 (1) ◽  
pp. 254
Author(s):  
Uppin Narayan Reddy ◽  
Swathi Chacham ◽  
Janampally Ravikiran ◽  
Jillalla Narsing Rao ◽  
Jakkampudi Nagasravani ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Female Child ◽  
Sinus Histiocytosis ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
Rare Case Report

scholarly journals Juvenile Peripheral Ossifying Fibroma – A rare case report and review

2021 ◽  
Vol 6 (3) ◽  
pp. 108-111
Author(s):  
Neha Saini ◽  
Varun Saini ◽  
Saurabh Jain ◽  
Tiny Jain
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Surgical Excision ◽  
Female Child ◽  
Tissue Response ◽  
Ossifying Fibroma ◽  
Orthodontic Appliances ◽  
Peripheral Ossifying Fibroma ◽  
Rare Case Report

 Peripheral ossifying fibroma, first reported by Shepard in 1844 as alveolar exostosis, is a non-neoplastic reactive lesion arising as a focal exophytic mass exclusively on the gingiva originating from the interdental area and shows no bone involvement in most cases. The lesion shows propensity for maxilla and incisor-cuspid region with female predilection. The etiological factors include local factors causing gingival irritation like calculus, plaque, ill fitting dentures or orthodontic appliances; and hormonal influence, initiate exhuberant connective tissue response. The lesion shows high recurrence potential , necessitating proper identification, treatment and effective long-term recall protocol. This case report presents a relatively rare case of juvenile peripheral ossifying fibroma in relation to mandibular central & lateral incisors in an adolescent female child followed for upto 1 year after surgical excision  

scholarly journals A Rare Case Report of Fatal Fulminant Hepatic Failure in a Child due to MixedvivaxandfalciparumInfection

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Neha Thakur ◽  
Ravitanaya Sodani ◽  
J. Chandra ◽  
Deonath Mahto
Keyword(s):  
Case Report ◽  
Fulminant Hepatic Failure ◽  
Hepatic Failure ◽  
Rare Case ◽  
Clinical Signs ◽  
Female Child ◽  
Peripheral Smear ◽  
Rare Case Report ◽  
Life Threatening ◽  
The Tropics

Malaria remains an overwhelming problem in the tropical developing countries, with 300 to 500 million new cases and about a million deaths per year (Mishra et al., 2003). Malaria is a potentially life-threatening disease in the tropics. Jaundice is one of the severe manifestations offalciparummalaria. Its incidence (Mishra et al., 2003). varies between 10 and 45% in different reports and is seen more in adults than in children. Jaundice may vary from mild to very severe. However, clinical signs of hepatic encephalopathy (such as liver flaps) are never seen unless there is presence of concomitant viral hepatitis (WHO, 2000). Our case is a 6-year-old female child presented with fever, jaundice, and anasarca. Peripheral smear showed trophozoites and schizonts ofPlasmodium(P.)vivaxand trophozoites and gametocytes ofP. falciparum.Viral markers for hepatitis were negative. She developed fulminant hepatic failure and expired after 26 hours of admission.

scholarly journals Nephrotic syndrome in a case of Rubinstein Taybi syndrome: a rare case report

2017 ◽  
Vol 5 (6) ◽  
pp. 2806
Author(s):  
Debasis Patro ◽  
Sunil Kumar Agarwalla ◽  
Nasreen Ali ◽  
Manaswinee Sahoo
Keyword(s):  
Nephrotic Syndrome ◽  
Case Report ◽  
Intellectual Disability ◽  
Rare Case ◽  
Female Child ◽  
Interesting Case ◽  
Facial Features ◽  
Severe Intellectual Disability ◽  
Current State ◽  
Rare Case Report

Rubinstein Taybi syndrome (RSTS) also known as Broad Thumb Hallux Syndrome characterized by distinct facial features with beaked or straight nose, short stature, moderate to severe intellectual disability, broad thumb and big toe. We report an interesting case of female child with history and examination suggestive of RSTS with Nephrotic syndrome. Investigation revealed presence of albumin in urine with hypercholesterolemia and hypoalbuminemia. Purpose of this case report is to highlight the distinctive presentation of this syndrome and to update the current state of knowledge.

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