HYPERZINCAEMIA AND HYPERCALPROTECTINAEMIA

Question 1

What is  HYPERZINCAEMIA AND HYPERCALPROTECTINAEMIA?

Accepted Answer

very rare
autosomal dominant
albumin gene mutation ? (OMIM (103600)
dysregulation of two members of the large S100 protein family [Sampson B et al. 2002]

Question 2

Gibt es eine deutsche Bezeichnung?

Accepted Answer

Hyperzinkämie und Hypercalprotectinämie

Question 3

What is the link to OMIM ?

Accepted Answer

OMIN 194470

Question 4

Which enzymes are involved?

Accepted Answer

?

Disease	HYPERZINCAEMIA AND HYPERCALPROTECTINAEMIA
Synonym	HYPERZINCEMIA, FAMILIAL DYSALBUMINEMIC
OMIM	194470 OMIM = Online Mendelian Inheritance of Men
Orphanet	251523
Gene locus	unknown
ICD	E83.2
Summary	very rare autosomal dominant albumin gene mutation ? (OMIM (103600) dysregulation of two members of the large S100 protein family [Sampson B et al. 2002]
Laboratory findings	Zinc inc (plasma)
Symptoms	onset, adolescent onset, childhood