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Submit PaperAnnals of Clinical and Medical Case Reports is a peer-reviewed journal that publishes original case reports covering various medical specialties. The journal aims to provide valuable insights and information on rare and interesting cases to help healthcare professionals improve patient care and outcomes.
Case studies give an indicate of the decision-making process so that other physicians can apply lateral thinking to their own cases. These speak to a significant, opportune and significant examination configuration in propelling clinical logical information, particularly of uncommon illnesses.
The publication of latest and emerging information in such a way to pave the platform for reporting of unique, unusual and rare cases enhance understanding of the disease process.
The article submission process typically involves selecting a journal or publication, formatting the article according to the guidelines provided, and submitting it through an online platform or via email. Once submitted, the article will undergo a peer review process where experts in the field evaluate its quality and relevance before a decision is made on whether to accept it for publication.
Authors are requested to submit an unpublished manuscript on our online portal submission form.
Journal prioritizes Plagiarism Checks to ensure the authenticity and originality of the content.
The article Review Process ensured rigorous evaluation and maintained the standard of excellence.
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Meet Our DoctorsGastrointestinal stromal tumors (GISTs) are rare tumors of the digestive tract, most commonly found in the stomach, with jejunal GISTs being particularly uncommon.t......
View PDF View FulltextThe concept of neoplastic dedifferentiation describes a process in which a population of malignant cells become so undifferentiated pathologically they resemble a more primitive cell line [1].......
View PDF View FulltextHuller-Scheie syndrome, one of the phenotypes of mucopolysaccharidosis type I (MPS I), is a rare autosomal recessive lysosomal storage disorder,.....
View PDF View FulltextSigmoid diverticular disease is a disease that can significantly reduce the quality of life. This work shows the course of therapy using manual methods available to a physiotherapist......
View PDF View FulltextClinical reasoning is fundamental in medical practice but faces significant challenges due to the increasing complexity and volume of medical information.....
View PDF View FulltextTuberculous otitis media (TOM) is rare and difficult to diagnose because of its low incidence and low suspicion. We experienced the patient with otorrhea and facial palsy and performed unnecessary operation because of delayed diagnosis with low suspicion. We report this case for the purpose of being helpful to other clinicians. ....
View PDF View FulltextParoxysmal nocturnal hemoglobinuria (PNH) is a rare hematologic disorder marked by intravascular hemolysis resulting from somatic cell mutations. The condition poses elevated risks of maternal and neonatal morbidity and mortality, w....
View PDF View FulltextIWe present a 70-year-old male, former smoker of 68 pack-years, without any other relevant personal or surgical history, nor any known allergies. He worked as a banana tree farmer. He came to our Pneumology....
View PDF View FulltextThe prognostic impact of poor nutritional status in severe encephalitis is not clearly understood. We aim to investigate the relationship betweenthe prognostic nutritional index (PNI) and poor outcomes of severe encephalitis. ....
View PDF View FulltextIn the ever-evolving landscape of clinical medicine, the significanceof case reports cannot be overstated. They serve as the building blocks of medical knowledge, offering valuable insights into rare conditions, unique presentations,...
View PDF View FulltextTo assess the epidemiological, clinical characteristics of Streptococcus mitis group (SMG) infections, their drug resistance profile, and their relative risk and prevalence for...
View PDF View FulltextTraumatic Cataract Is a serious and common condition that mainly affects young adults and children. We report the case of a 25-year-old femalepatient who presented for consultation with blurred vision that had...
View PDF View FulltextGlobal urbanization and the events of the COVID-19 pandemic have revealed problems related to the consequences of disturbed ecology and weakened immunity of residents of megacities. According to experts of the International Monetary Fund, the financial losses of the global economy...
View PDF View FulltextRetrograde Type A aortic dissection is a rare but potentially life-threatening complication of thoracic endovascular aortic repair (TEVAR). A 61-yearold man presented with...
View PDF View FulltextIn recent years, the introduction of drug-eluting stents(DES) in PCIs (Percutaneous Coronary Interventions) for coronary...
View PDF View FulltextSpontaneous coronary artery dissection (SCAD) is a rare and emergent condition where a tear in the intimal portion of the coronary artery produces ischemia to the myocardium...
View PDF View FulltextBone formation or ossification in skin is a rare phenomenon that may be primary or secondary. Primary cutaneous ossification is mainly seen in Albright hereditary ...
View PDF View FulltextThe correlation between short-chain fatty acids (SCFAs) in the intestinal flora and sarcopenia in patients with type 2 diabetes is a topic of growing interest in recent research...
View PDF View FulltextHyperparathyroidism with diffuse bone lesions is relatively rare, typically manifesting with symptoms such as bone pain or pathologic fractures. Due to the lack of understanding of this disease, these extensive lytic lesions are often misdiagnosed...
View PDF View FulltextBrucellosis is a bacterial endemic zoonotic disease of global significance with detrimental impacts on public health and food animal production. It is caused by Brucella spp., an expanding group of pathogens able to infect various host species...
View PDF View FulltextThe aim of this study is to compare dental and skeletal effects in Herbst appliance treatment without anchorage, with interradicular skeleta...
View PDF View FulltextDeafness-Dystonia Syndrome (DDS) is a rare and complicated disorder which can be caused by a pathogenic heterozygous mutation c.547C>T, p.(Arg183Trp) in the ACTB gene, typically leading to a combination of hearing impairment and dystonia...
View PDF View FulltextMost children with cystic fibrosis suffer from secondary chronic rhinosinusitis for which current treatment options are limited. Novel treatment for cystic fibrosis targeting the cause of the disease shows big promise in increasing pulmonary function...
View PDF View FulltextAntineutrophil cytoplasmic antibodies (ANCA) are the serological hallmark of some idiopathic systemic vasculitis, Pauci-immune necrotizing and crescentic glomerulonephritis (NCGN) is a frequent component of ANCA-associated vasculitis....
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