Nonspherocytic haemolytic anaemia due to hexokinase deficiency (Q99644): Difference between revisions

@@ description / pt-br / description / pt-br @@
+Anemia hemolítica não esferocítica devido a deficiência de hexoquinase é caracterizada por hemólise grave, tendo início na infância. _x000D_ Dezessete famílias afetadas foram relatadas até o momento. A transmissão é autossômica recessiva. As mutações foram descritas no HK1, o gene que codifica a hexoquinase-R específica dos glóbulos vermelhos.
@@ description / en / description / en @@
+Nonspherocytic haemolytic anaemia due to hexokinase deficiency is characterised by severe haemolysis, appearing in infancy. Seventeen affected families have been reported so far. Transmission is autosomal recessive. Mutations have been described in HK1, the gene that encodes red blood cell-specific hexokinase-R.
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+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
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@@ Property / Collection date: 15 August 2026 / rank @@
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Latest revision as of 16:19, 16 August 2026

Nonspherocytic haemolytic anaemia due to hexokinase deficiency is characterised by severe haemolysis, appearing in infancy. Seventeen affected families have been reported so far. Transmission is autosomal recessive. Mutations have been described in HK1, the gene that encodes red blood cell-specific hexokinase-R.

Language	Label	Description	Also known as
default for all languages	ID_1942043262
English	Nonspherocytic haemolytic anaemia due to hexokinase deficiency	Nonspherocytic haemolytic anaemia due to hexokinase deficiency is characterised by severe haemolysis, appearing in infancy. Seventeen affected families have been reported so far. Transmission is autosomal recessive. Mutations have been described in HK1, the gene that encodes red blood cell-specific hexokinase-R.