Thiamine responsive megaloblastic anemia syndrome
Overview
A rare genetic disorder characterized by megaloblastic anemia, hearing loss and diabetes. The condition is caused by a deficiency of a thiamine (vitamin B1) transporter protein which means that the body is unable to effectively utilize thiamine from the diet.
Symptoms
* Megaloblastic anemia * Nerve deafness * Transposition of abdominal organs * Enlarged liver * Enlarged spleen
Prognosis
The 'prognosis' of Thiamine responsive megaloblastic anemia syndrome usually refers to the likely outcome of Thiamine responsive megaloblastic anemia syndrome. The prognosis of Thiamine responsive megaloblastic anemia syndrome may include the duration of Thiamine responsive megaloblastic anemia syndrome, chances of complications of Thiamine responsive megaloblastic anemia syndrome, probable outcomes, prospects for recovery, recovery period for Thiamine responsive megaloblastic anemia syndrome, survival rates, death rates, and other outcome possibilities in the overall prognosis of Thiamine responsive megaloblastic anemia syndrome. Naturally, such forecast issues are by their nature unpredictable.
Treatment
* Womens Health Specialists: o Obstetrics & Gynecology o Reproductive Endocrinology & Infertility o Gynecological Oncology o Maternal & Fetal Medicine o Neonatal-Perinatal Medicine * Blood Health Specialists (Hematology): o Hematology (Blood Specialists) o Pediatric Hematology / Oncology (Child Cancer/Leukemia) o Hematopathology