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  • Pediatrics and Neonatology
  • Pediatrics and...

Pediatrics and Neonatology Cases - Page 2

Off-label use of otic ciprofloxacin/dexamethasone led to hyperglycemia in infant: Case report

Off-label use of otic ciprofloxacin/dexamethasone led to hyperglycemia in infant: Case report

Medha Baranwal20 Jun 2022 10:15 AM IST
USA: A recent case report, published in the Annals of Otology, Rhinology & Laryngology, describes the case of hyperglycemia in a child with Type 1...
Surgeons transplant 3D ear made of living cells

Surgeons transplant 3D ear made of living cells

Dr. Kamal Kant Kohli6 Jun 2022 8:00 PM IST
Washington: A US medical team said Thursday they had reconstructed a human ear using the patient's own tissue to create a 3D bioimplant, a pioneering...
Case study suggests connection of  COVID-19 with croup among infants

Case study suggests connection of COVID-19 with croup among infants

Medha Baranwal28 May 2022 9:15 AM IST
Turkey: A research brief and a case report published in Pediatric Infectious Disease Journal have indicated a connection between croup and COVID-19 in...
Rare case of childhood bullous pemphigoid mimicking toxic epidermal necrolysis: a report

Rare case of childhood bullous pemphigoid mimicking toxic epidermal necrolysis: a report

Medha Baranwal12 May 2022 8:30 PM IST
Iran: A recent case study in the journal Case Reports in Dermatological Medicine describes the case of a childhood bullous pemphigoid (BP) that...
A Novel Mutation Causing Primary Hypoaldosteronism In a Term Neonate: Case report

A Novel Mutation Causing Primary Hypoaldosteronism In a Term Neonate: Case report

dr anusha15 Jan 2022 3:00 PM IST
A team of neonatologists from Fernandez Hospital,Hyderabad reported an interesting case of primary hypoaldosteronism as a consequence of rare gene...
A Rare Case of Taloromyces Marneffei Infection In A HIV child-BMC case report

A Rare Case of Taloromyces Marneffei Infection In A HIV child-BMC case report

dr anusha13 Jan 2022 9:00 AM IST
Talaromyces Marneffei (Penicillium marneffei, T.marneffei) has been frequently reported in patients with adult acquired immunodeficiency syndrome....
Atypical presentation of MIS-C in a neonate:BMJ case report

Atypical presentation of MIS-C in a neonate:BMJ case report

dr anusha25 Dec 2021 9:00 AM IST
Researchers from Delhi present the first case report of a neonate presenting within 48 hours of life with predominant abdominal signs mimicking...
Propranolol benefits infantile tremor syndrome after initiating vitamin B12 therapy: Case Study

Propranolol benefits infantile tremor syndrome after initiating vitamin B12 therapy: Case Study

Dr. Shravani Dali22 Dec 2021 9:00 AM IST
Propranolol is beneficial for the treatment of infantile tremor syndrome (ITS) in the context of vitamin B12 deficiency, according to a recent case ...
Ketorolac not significantly related to bleeding risk in kids operated for perforated appendicitis

Ketorolac not significantly related to bleeding risk in kids operated for perforated appendicitis

MD Editorial Team13 Dec 2021 9:00 AM IST
Ketorolac is an opioid-sparing medication that is commonly used in children. Ketorolac, on the other hand, should be avoided in children with...
Maternal hypothyroidism closely related with Cardiovascular Diseases in Offspring: Study

Maternal hypothyroidism closely related with Cardiovascular Diseases in Offspring: Study

MD Editorial Team10 Dec 2021 9:00 AM IST
Maternal hypothyroidism is associated with an increased risk of CVD in offspring, according to a new study led by Maohua Miao and colleagues. Thyroid...
Rare case of cerebral infarction in Congenital Adrenal Hyperplasia: A report

Rare case of cerebral infarction in Congenital Adrenal Hyperplasia: A report

dr anusha2 Nov 2021 9:00 AM IST
Congenital Adrenal Hyperplasia is an autosomal recessive inherited disorder of steroid synthesis pathway and remains the commonest cause of primary...
Mumbai: 2.5-Year-Old Child Underwent Cellular Therapy for a Rare Disorder - Joubert Syndrome

Mumbai: 2.5-Year-Old Child Underwent Cellular Therapy for a Rare Disorder - Joubert Syndrome

Dr. Kamal Kant Kohli25 Oct 2021 9:00 AM IST
Mumbai: Dr. Pradeep Mahajan, Regenerative Medicine Researcher, StemRx Bioscience Pvt. Ltd. gives a ray of hope to a 2.5-year-old child suffering from...
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