|
8p11.2 Google OMIM Orphanet PubMed Wikipedia Spherocytosis, hereditary *Gene map locus 8p11.2 HS Spherocytosis, severe atypical, due to suspected ankyrin defect [Clinical features: spherocytosis; hemolytic anemia; splenomegaly] [Inheritance: autosomal dominant] |
![]() |
![]() |
![]() |
|
Red blood cells, spherocytosis |
Hereditary spherocytosis |
Splenomegaly in spherocytosis (laparoscopic view) |
|
MedlinePlus |
New England Journal of Medicine |
Pediatric Surgery - Brown Medical School |
![]() |
![]() |
|
|
Splenomegaly in spherocytosis (laparoscopic view) |
Spherocytes |
|
|
Pediatric Surgery - Brown Medical School |
Wadsworth Center, NYS Department of Health |