Ajinkya Wazurkar
Overview
Explore the profile of Ajinkya Wazurkar including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
10
Citations
0
Followers
0
Related Specialty
Related Specialty
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Wandile S, Waghmode M, Uke P, Vagha J, Javvaji C, Wazurkar A
Cureus
. 2024 Aug;
16(7):e65714.
PMID: 39211640
Background: Neonatal morbidity and mortality continue to be major public health issues globally, especially for infants admitted to neonatal intensive care units (NICUs). This study aims to investigate the incidence...
2.
Bhatnagar A, Velagala V, Vagha J, Lohiya S, Wazurkar A, Wandile S, et al.
Cureus
. 2024 Aug;
16(7):e64951.
PMID: 39161514
Type 2 respiratory failure, or hypercapnic respiratory failure, is brought on by low oxygenation (hypoxemia) and inadequate breathing (hypercapnia). It is produced by factors that can create an imbalance between...
3.
Kommareddy A, Vagha K, Vagha J, Javvaji C, Taksande A, Meshram R, et al.
Cureus
. 2024 Aug;
16(7):e63766.
PMID: 39100022
Background Congenital anomalies of the kidney and urinary tract (CAKUT) encompass a diverse array of disorders arising from developmental irregularities in the renal parenchymal development, disrupted embryonic migration of the...
4.
Wandile S, Vagha J, Wazurkar A, Lohiya S, Hinge D, Javvaji C, et al.
Cureus
. 2024 Jul;
16(6):e63005.
PMID: 39055408
Chylothorax is a severe complication following the Fontan procedure, causing significant morbidity and mortality due to nutritional depletion and fluid loss. We present a case involving a six-year-old girl with...
5.
Velagala V, Bhatnagar A, Vagha J, Lohiya S, Wazurkar A, Wandile S, et al.
Cureus
. 2024 Jul;
16(6):e61700.
PMID: 38975552
Biliary ascites due to spontaneous biliary duct perforation is a rare case presentation usually seen in the paediatric age group of 6-36 months. We are presenting the case of a...
6.
Kommareddy A, Raut V, Vagha K, Javvaji C, Varma A, Vagha J, et al.
Cureus
. 2024 Jun;
16(5):e60720.
PMID: 38903295
Congenital complete heart block (CCHB) is a rare and potentially life-threatening condition, often associated with maternal autoantibodies. We present the case of a one-year-old girl with recurrent respiratory symptoms, ultimately...
7.
Vagha J, Wazurkar A, Madke B, Lohiya S, Wandile S, Vagha K, et al.
Cureus
. 2024 Jun;
16(5):e59510.
PMID: 38826988
A rare autosomal recessive condition called infantile systemic hyalinosis (ISH) is characterized by early-onset skin lesions that progress to the formation of numerous contractures. The underlying disease is the progressive...
8.
Vagha K, Lohiya S, Vagha J, Hampe P, Wazurkar A, Malik A, et al.
Cureus
. 2024 Mar;
16(2):e54871.
PMID: 38533162
Wilson disease (WD) is an autosomal recessive disorder marked by aberrations in copper metabolism, leading to its accumulation in vital organs such as the liver, brain, cornea, kidneys, and heart....
9.
Vagha J, Wazurkar A, Vagha K, Lohiya S, Varma A
Cureus
. 2023 May;
15(4):e37411.
PMID: 37181966
Hypertelorism and hypospadias are the main characteristics of telecanthus-hypospadias syndrome; however, it can also include other midline structural anomalies, such as cleft lip and palate, cryptorchidism, congenital heart problem, laryngotracheal...
10.
Sarda P, Vagha K, Kenjale S, Singh K, Wazurkar A, Ganvir S, et al.
Cureus
. 2022 Dec;
14(10):e30760.
PMID: 36457643
An uncommon autosomal dominant condition known as Crouzon's syndrome causes abnormalities of the skull and face. It accounts for 4.8% of all cases of craniosynostosis and is by far the...