Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1093/ajcp/62.4.461 | DOI Listing |
Similar Publications
Microcytosis Merits Evaluation: A Case Report of Hemoglobin S With Hereditary Persistence of Fetal Hemoglobin (HbS-HPFH Syndrome).
Cureus
February 2025
Hematology-Oncology, Veterans Affairs Greater Los Angeles Health System, Los Angeles, USA.
Microcytosis is commonly encountered in primary care. Among patients with normal iron stores or compatible family history, hemoglobin electrophoresis, traditionally performed with gel electrophoresis and now through combination capillary electrophoresis/high-performance liquid chromatography, can diagnose thalassemic disorders or, rarely, a hemoglobinopathy. We present a case of an incidentally discovered microcytosis in a 34-year-old male patient where the workup led to a diagnosis of Hemoglobin S with Hereditary Persistence of Fetal Hemoglobin (HbS-HPFH syndrome).
View Article and Find Full Text PDFPurpose: The prevalence of carpal tunnel syndrome (CTS) as the foremost upper extremity entrapment neuropathy is well-documented. The present study aimed to evaluate the prevalence of anatomical variations in the carpal tunnel and their potential role as risk factors for CTS.
Methods: Data from 447 CTS patients who underwent median nerve decompression between 2018 and 2019 were retrospectively analyzed.
Purpose: This study aimed to conduct a radiological and clinical evaluation of patients who underwent fixed rehabilitation involving subperiosteal implants and to define not only the criteria for failure but also the criteria for survival and success.
Materials And Methods: Patients suffering from severe atrophy of the maxilla and/or mandible underwent immediate loading with fixed full-arch prostheses supported by custom-made 3D-printed subperiosteal implants. The evaluated outcomes included the success and survival rates of subperiosteal implant prosthetic therapy, surgical complications, and the three-dimensional positions of osteosynthesis screws and sleeves used for implant adhesion to the bone.
Challenge in a Malrotation Case: Presentation Mimicking Severe Combined Immunodeficiency.
J Paediatr Child Health
March 2025
Ihsan Dogramaci Children Hospital, Hacettepe University, Ankara, Turkey.
Objectives: Malrotation is a congenital anomaly characterized by improper positioning of the intestines that can cause a range of symptoms from asymptomatic to life-threatening, including midgut volvulus. Diagnosis of malrotation can be particularly challenging in cases where symptoms resemble those of other illnesses, such as severe combined immunodeficiency (SCID).
Case Report: In this case study, we describe a 2-month-old girl with midgut volvulus secondary to malrotation.
Conservative approach to a rare case of persistent sciatic artery with iatrogenic femoral arteriovenous fistula: a case report.
Front Surg
February 2025
Department of Vascular Surgery, Tianjin First Central Hospital, Tianjin, China.
Persistent sciatic artery (PSA) is a rare anatomic variant disease with an incidence of approximately 0.025%-0.05% it is considered to be an axial congenital vascular malformation, which may be related to the failure of sciatic artery degeneration and iliofemoral artery dysplasia.
View Article and Find Full Text PDFWant AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!
© LitMetric 2025. All rights reserved.