Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis.

Authors :: Fortugno C
Galea E
Cantaffa R
Gigliotti F
Fabiano RL
Talarico V
Raiola G
Galati MC
Source :: Pediatric hematology and oncology [Pediatr Hematol Oncol] 2021 Mar; Vol. 38 (2), pp. 184-190. Date of Electronic Publication: 2020 Nov 02.
Publication Year :: 2021

Subjects :: Child, Preschool
Humans
Male
Mutation
Anemia, Hemolytic, Congenital blood
Cell Membrane pathology
Erythrocytes pathology
Hydrops Fetalis blood
Spherocytosis, Hereditary genetics

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