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Article

Cold-induced sweating syndrome: CISS1 and CISS2: manifestations from infancy to adulthood. Four new cases.

Journal of the neurological sciences - 15 Jun 2010

Hahn A F, Waaler P E, Kvistad P H, Bamforth J S, Miles J H, McLeod J G, Knappskog P M, Boman H

Abstract excerpt

Cold-induced sweating syndrome (CISS), a rare autosomal recessive disorder, is genetically heterogeneous. Deficiency of the CRLF1 and the CLCF1 gene functions results in CISS1 and CISS2, respectively. So far, only a single patient with CISS2 has been reported. Here we describe four new cases of CISS, two additional patients with CISS2 (confirming locus heterogeneity) and two patients with CISS1. Their case...

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Source

Identifiers

PMID: 20400119
DOI: 10.1016/j.jns.2010.02.028

Genes

CLCF1
CRLF1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Cold-induced sweating syndrome: CISS1 and CISS2: manifestations from infancy to adulthood. Four new cases.PMID 20400119Read ↗

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