KAHRAMANMARAS SUTCU IMAM UNIVERSITY
Health Practice and Research Hospital
🩺 Geriatrics Clinic Our Geriatrics Clinic, which aims to protect the physical, mental and social health of elderly individuals, offers a holistic evaluation and treatment service to our elderly patients with its experienced physician staff.
❤️ Pediatric Cardiology Clinic We offer safe, comfortable and modern healthcare services to our children with our expert team in the diagnosis and treatment of congenital or acquired heart diseases.
🎗️ Oncology Clinic Our Oncology Clinic, which provides services with state-of-the-art devices and a multidisciplinary approach in cancer diagnosis and treatment, aims to offer our patients a hopeful recovery process.
🩸 Hematology Clinic Specializing in the diagnosis, treatment and follow-up of blood diseases, our Hematology Clinic provides personalized care to its patients in line with scientific and ethical values.
Annual total inspection data
Definition: Pancreatitis is a serious disease caused by inflammation of the pancreas. Symptoms: Severe abdominal pain, nausea and vomiting, fever, and abdominal tenderness. Causes: Gallstones, alcohol use. Diagnosis:
Definition Pulmonary hypertension is a disease characterized by increased pressure in the lung vessels. Symptoms Shortness of breath Fatigue Chest pain Fainting Causes Heart diseases, lung diseases, primary pulmonary
Definition Schmid metaphyseal chondrodysplasia is a rare skeletal dysplasia characterized by short stature, genu varum, and metaphyseal dysplasia. Symptoms Short stature Genu varum Metaphyseal dysplasia Gait
Definition: Tetralogy of Fallot is a complex congenital heart disease characterized by four distinct heart anomalies. Symptoms: Cyanosis, Shortness of breath, Squatting position, Growth retardation, Causes: Congenital development
Definition Geleophysic dysplasia is a rare skeletal dysplasia characterized by short stature, characteristic face, and progressive cardiac disease. Symptoms Short stature, characteristic face, progressive cardiac disease
Definition: Huntington disease is a progressive neurodegenerative inherited disorder. Symptoms: Choreiform movements, cognitive impairment, behavioral changes, difficulty swallowing. Causes: HTT gene mutation. Diagnosis: Genetic testing. Treatment:
