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hereditary spherocytic hemolytic Anemia

A rare hereditary form of spherocytosis caused by mutations in the ANKYRIN -1 gene (OMIM: 612641). Symptoms include jaundice, excessive fatigue, and delayed puberty.
Also Known As:
Anemia, hereditary spherocytic hemolytic; Acholuric jaundice; Chronic acholuric jaundice; Congenital hemolytic jaundice; Debrie's familial haemolytic disease; Minkowski-Chauffard disease; Minkowski-Chauffard haemolytic jaundice; Minkowski-Chauffard-Gänsslen syndrome
Networked: 29 relevant articles (1 outcomes, 2 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Splenomegaly
2. Thrombosis (Thrombus)
3. Jaundice (Icterus)
4. Hepatomegaly
5. Hemorrhage

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to hereditary spherocytic hemolytic Anemia:
1. amsonic acid (DAS)IBA

Therapies and Procedures

1. Splenectomy
2. Nursing Care
3. Therapeutics
4. Blood Transfusion (Blood Transfusions)