A5006738255- Hemoglobinopathies and Related Disorders
- Congenital limb and hand anomalies
- Genomic variations and chromosomal abnormalities
- Hedgehog Signaling Pathway Studies
- RNA modifications and cancer
- Iron Metabolism and Disorders
- Monoclonal and Polyclonal Antibodies Research
- Urological Disorders and Treatments
- Contact Dermatitis and Allergies
- Clinical Nutrition and Gastroenterology
- Congenital Ear and Nasal Anomalies
- Pharmaceutical Practices and Patient Outcomes
- Prenatal Screening and Diagnostics
- Polyamine Metabolism and Applications
- Nausea and vomiting management
- Epigenetics and DNA Methylation
- Fetal and Pediatric Neurological Disorders
- Food Allergy and Anaphylaxis Research
- Colorectal and Anal Carcinomas
- DNA and Nucleic Acid Chemistry
- Drug-Induced Adverse Reactions
- Health Literacy and Information Accessibility
- Neurogenetic and Muscular Disorders Research
- Cleft Lip and Palate Research
- Pediatric Urology and Nephrology Studies
Shri Maharaja Hari Singh Hospital
2024
Ministry of Health
2019
Centre for Arab Genomic Studies
2006-2011
Canadian University of Dubai
2006
Sanjay Gandhi Post Graduate Institute of Medical Sciences
1992-1996
<h3>Background</h3> Split-hand/foot malformation (SHFM)—also known as ectrodactyly—is a congenital disorder characterised by severe malformations of the distal limbs affecting central rays hands and/or feet. A distinct entity termed SHFLD presents with SHFM and long bone deficiency. Mouse models suggest that defect apical ectodermal ridge leads to phenotype. Although six different loci/mutations (SHFM1–6) have been associated SHFM, underlying cause in large number cases is still unresolved....
Background: Postpartum vesicovaginal fistulas (VVFs) are a significant complication of childbirth, particularly in low-resource settings, leading to long-term physical and psychosocial challenges for affected women. Objective: This study aims identify the key risk factors, assess effectiveness prevention strategies, evaluate surgical treatment outcomes postpartum VVFs. Methods: retrospective cohort was conducted at Avicenna Hospital, Lahore, July December 2024. A total 123 women diagnosed...
Abstract We report on a newborn boy with Neu‐Laxova syndrome and spina bifida, bilateral cryptorchidism, shallow orbital cavities. Asso‐ciation of these manifestations in is the first to be reported literature. This from India.
Abstract Ectrodactyly with aplasia of long bones syndrome is one the most recognizable defects involving extremities. We have studied a very large eight‐generation consanguineous Arab family from United Emirates (UAE) multiple severe limb anomalies resembling this condition (OMIM; 119100), for which affected gene unknown. The pedigree consists 145 individuals including 23 (14 males/9 females) anomalies. Of these, 18 had tibial (TA) usually on right side. expression phenotype was variable and...
Abstract We present 2 unrelated fetuses with manifestations of both the hydrolethalus syndrome and short rib‐polydactyly syndrome, type Majewski. It is proposed that cases limbs constitute a separate lethal osteochondrodysplasia mimicking syndromes. © 1992 Wiley‐Liss, Inc.
β-Thalassemia (β-thal) is characterized by the absent or reduced production of β-globin chains. The precise molecular lesion that causes decreased synthesis in β+-thal difficult to predict when mutations occur locus control region (LCR), promoter, introns 3′ untranslated regions (3′UTRs). Among them, role 3′UTR gene mRNA stability poorly understood, mainly due very few cases have this region. So far, only three been reported gene. Although, it speculated some these could be associated with...
Patients with allergy to multiple drugs who have experienced anaphylaxis times present a significant challenge in perioperative management. This report presents 27-year-old female patient diagnosed cholelithiasis scheduled for cholecystectomy. The has history of adverse reaction drugs, including Amoxicillin/Clavulanic acid, Cefpodoxime, Levofloxacin and two additional (one analgesic the other multivitamin) each resulting symptoms suggestive on separate occasions. However, demonstrated...
Purpose: The study aimed to assess the outcome and safety of PCCL in pediatric population coming with bladder stones developing countries.
 Methodology: Patients age vesical calculus were evaluated for PCCL. Department Peads Urology Institute Kidney Diseases Thirty participants included single center study, enrollment beginning January 2000 ending August 2021. General anesthesia was used operation. Following a cystoscopy examination, suprapubic puncture performed, urethral tract dilated...
Abstract This article reports on efforts to overcome common hurdles that were faced during population‐based screening for hemoglobinopathies in the United Arab Emirates. An Internet‐based approach was designed and implemented increase acceptance of program. The process involved: an awareness campaign, a simple bilingual (Arabic/English) online consent form registration process, use barcode sample labeling, equipment upgrade, electronic communication successful test results, counseling...
Haemoglobin disorders are hereditary, lifelong and characterised by the need for multifaceted management. The question of quality in meeting standards care that likely to bring best possible outcomes patients is a necessary consideration. concept reference centres supporting peripheral treatment formal networking relationship response real needs practical solution public health terms. In this report, team advisors Thalassaemia International Federation (TIF) attempts suggest set...
Objectives To investigate the impact of electronic medical record (EMR) on improvement healthcare parameters in a thalassaemia centre located at Fujairah Hospital, Fujairah, UAE. Materials and methods A hospital-wide EMR system (Wareed) was implemented across hospitals Ministry Health Prevention, UAE, including two major centres. We aim to this intervention number over quarters (before after implementation system). Results Since preimplementation data were not available for one facility,...
Background: Patients with transfusion dependent beta thalassemia major develop a number of complications whichhypogonadism is the most common. In addition, raised serum ferritin level has been associated hypogonadism.Objective: To determine correlation between ferritin, gonadotrophins and sex hormones in patients transfusiondependent â-thalassemia syndrome patients.Material methods: This cross sectional study was designed conducted at Institute Basic Medical Sciences (IBMS),Khyber University...