A dual left anterior descending (LAD) artery is a rare congenital anomaly which is classified into different types based on the origin, course and termination of the short and long LAD arteries. To date, 10 variants of dual LAD artery anomalies have been described. We report a 44-year-old woman who was referred to the Department of Radiology, Royal Hospital, Muscat, Oman, in 2017. Coronary computed tomography angiography revealed a dual LAD artery anomaly in which the short and long LAD arteries shared a common ostium with the right coronary artery from the right coronary sinus. To the best of the authors’ knowledge, this type of variant has not been previously reported in the literature.Keywords: Coronary Angiography; Congenital Abnormalit...
First discovered by Friedenstein in 1976, mesenchymal stem cells (MSCs) are adult stem cells found t...
Spinal muscular atrophy (SMA) is a genetic lower motor neuron disease. It usually involves all of th...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...
A dual left anterior descending (LAD) artery is a rare congenital anomaly which is classified into d...
Myxomas originating from the aortic valve are rare. We report a 40-year-old male patient who present...
A salivary gland anlage tumour (SGAT) is a very rare type of benign tumour that usually presents in ...
Dermatofibrosarcomas protuberans (DFSP) are rare low-grade tumours with various subtypes and usually...
Acute polyneuropathy is a rare manifestation of severe hyperthyroidism. We report a 22-year-old Oman...
Macrodystrophia lipomatosa (ML) is a rare congenital non-hereditary condition caused by an increase ...
It has been a well-known practice to use seeds and the essential oil of Carum copticum as a strongly...
Congenital contractural arachnodactyly, commonly known as Beal’s syndrome, is an extremely rare gene...
A group of amine derivatives [4-aminobenzenesulfonamide derivatives, 2-aminopyridine and 2-aminothia...
Plasma cell leukaemia (PCL) is one of the most aggressive and rarest forms of plasma cell dyscrasia....
Matrix stones are a rare form of urinary calculi with a low mineral content. We report a 63-year-old...
Multiple myeloma (MM) is an uncommon malignancy characterised by the proliferation of clonal plasma ...
First discovered by Friedenstein in 1976, mesenchymal stem cells (MSCs) are adult stem cells found t...
Spinal muscular atrophy (SMA) is a genetic lower motor neuron disease. It usually involves all of th...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...
A dual left anterior descending (LAD) artery is a rare congenital anomaly which is classified into d...
Myxomas originating from the aortic valve are rare. We report a 40-year-old male patient who present...
A salivary gland anlage tumour (SGAT) is a very rare type of benign tumour that usually presents in ...
Dermatofibrosarcomas protuberans (DFSP) are rare low-grade tumours with various subtypes and usually...
Acute polyneuropathy is a rare manifestation of severe hyperthyroidism. We report a 22-year-old Oman...
Macrodystrophia lipomatosa (ML) is a rare congenital non-hereditary condition caused by an increase ...
It has been a well-known practice to use seeds and the essential oil of Carum copticum as a strongly...
Congenital contractural arachnodactyly, commonly known as Beal’s syndrome, is an extremely rare gene...
A group of amine derivatives [4-aminobenzenesulfonamide derivatives, 2-aminopyridine and 2-aminothia...
Plasma cell leukaemia (PCL) is one of the most aggressive and rarest forms of plasma cell dyscrasia....
Matrix stones are a rare form of urinary calculi with a low mineral content. We report a 63-year-old...
Multiple myeloma (MM) is an uncommon malignancy characterised by the proliferation of clonal plasma ...
First discovered by Friedenstein in 1976, mesenchymal stem cells (MSCs) are adult stem cells found t...
Spinal muscular atrophy (SMA) is a genetic lower motor neuron disease. It usually involves all of th...
ABSTRACT: Pulmonary hyalinising granuloma (PHG) is a rare fibrosclerosing inflammatory lung conditio...