Sweat volume quantification in paediatric population
Corresponding Author
S. Hadj-Rabia
Department of Dermatology and Reference Center for Rare Skin Diseases, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
INSERM U1163, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Paris, France
Correspondence
S. Hadj-Rabia, Department of Dermatology, Hôpital Universitaire Necker-Enfants Malades, AP-HP Centre Université Paris Cité, 149 rue de Sèvres – 75743 Paris Cedex 15, France.
Email: [email protected]
Search for more papers by this authorT. Nguyen-Khoa
Laboratory of Biochemistry, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
Laboratory of the Ile-de-France Newborn Screening, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
Reference Center for Rare Diseases: Cystic Fibrosis and Other Epithelial Respiratory Protein Misfolding Diseases, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
INSERM U1151, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France
Search for more papers by this authorJ. Mashiah
Department of Dermatology and Reference Center for Rare Skin Diseases, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
Division of Dermatology, Pediatric Dermatology Clinic, Dana-Dwek Children's Hospital, Israel Sourasky Medical Center, Tel Aviv, Israel
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorCorresponding Author
S. Hadj-Rabia
Department of Dermatology and Reference Center for Rare Skin Diseases, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
INSERM U1163, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Paris, France
Correspondence
S. Hadj-Rabia, Department of Dermatology, Hôpital Universitaire Necker-Enfants Malades, AP-HP Centre Université Paris Cité, 149 rue de Sèvres – 75743 Paris Cedex 15, France.
Email: [email protected]
Search for more papers by this authorT. Nguyen-Khoa
Laboratory of Biochemistry, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
Laboratory of the Ile-de-France Newborn Screening, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
Reference Center for Rare Diseases: Cystic Fibrosis and Other Epithelial Respiratory Protein Misfolding Diseases, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
INSERM U1151, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France
Search for more papers by this authorJ. Mashiah
Department of Dermatology and Reference Center for Rare Skin Diseases, Hôpital Necker-Enfants Malades, AP-HP Centre Université Paris Cité, Paris, France
Division of Dermatology, Pediatric Dermatology Clinic, Dana-Dwek Children's Hospital, Israel Sourasky Medical Center, Tel Aviv, Israel
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel
Search for more papers by this authorOpen Research
DATA AVAILABILITY STATEMENT
The data that support the findings of this study are available from the corresponding author upon reasonable request.
REFERENCES
- 1Baker LB, Wolfe AS. Physiological mechanisms determining eccrine sweat composition. Eur J Appl Physiol. 2020; 120: 719–752.
- 2Cirilli N, Southern KW, Barben J, Vermeulen F, Munck A, Wilschanski M, et al. Standards of care guidance for sweat testing; phase two of the ECFS quality improvement programme. J Cyst Fibros. 2022; 21: 434–441.
- 3Burat B, Reynaerts A, Baiwir D, Fléron M, Eppe G, Leal T, et al. Characterization of the human eccrine sweat proteome – a focus on the biological variability of individual sweat protein profiles. Int J Mol Sci. 2021; 22: 10871.
- 4Schneider H, Schweikl C, Faschingbauer F, Hadj-Rabia S, Schneider P. A causal treatment for X-linked hypohidrotic ectodermal dysplasia: long-term results of short-term perinatal ectodysplasin A1 replacement. Int J Mol Sci. 2023; 24: 7155.
- 5Peschel N, Wright JT, Koster MI, Clarke AJ, Tadini G, Fete M, et al. Molecular pathway-based classification of ectodermal dysplasias: first five-yearly update. Genes (Basel). 2022; 13: 2327.
- 6Oshima Y, Fujimoto T, Nomoto M, Fukui J, Ikoma A. Hyperhidrosis: a targeted literature review of the disease burden. J Dermatol. 2023; 50: 1227–1236.
- 7Schneider H, Faschingbauer F, Schuepbach-Mallepell S, Körber I, Wohlfart S, Dick A, et al. Prenatal correction of X-linked hypohidrotic ectodermal dysplasia. N Engl J Med. 2018; 378: 1604–1610.