Other names: Diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy
Cutaneous phenotype of Naxos disease: woolly hair (A), palmar (B) and plantar (C) keratoses.
Naxos disease (also known as "diffuse non-epidermolytic palmoplantar keratoderma with woolly hair and cardiomyopathy,"[1] "diffuse palmoplantar keratoderma with woolly hair and arrhythmogenic right ventricular cardiomyopathy, first described on the island of Naxos by Nikos Protonotarios,"[1] and "Naxos disease"[1]) is a cutaneous condition characterized by a palmoplantar keratoderma.[1] The prevalence of the syndrome is up to 1 in every 1000 people in the Greek islands.[2]
It has been associated with mutations in the genes encoding the proteins desmoplakin, plakoglobin, desmocollin-2, and SRC-interacting protein (SIP).[3][4] A variation of Naxos syndrome is known as Carvajal syndrome.[2]
Contents
1Symptoms and signs
2Cause
3Management
4See also
5References
6External links
Symptoms and signs[edit | edit source]
a) Striate palmar keratoderma, b) striate plantar keratoderma
Between 80 and 99% of those with Naxos disease will display some of the following symptoms:r[5]
Disease of the heart muscle
Thickening of palms and soles
Sudden increased heart rate
Dizzy spells
Kinked hai
Cardiomegaly
Dilated cardiomyopathy
Detachment of nail
Sparse body hair
Cause[edit | edit source]
DSP
The desmosomal proteins plakoglobin and desmoplakin take on mutations that cause Naxos disease. [6]
Increased mechanical stress leads to cell death, due to defects in linking sites of plakoglobin and desmoplakin which can interrupt series of cell adhesion[6]
Management[edit | edit source]
The treatment for this condition is based on the following:[6]
Automatic cardioverter defibrillator
Antiarrhythmic drugs
Heart transplantation
See also[edit | edit source]
Olmsted syndrome
List of cutaneous conditions
List of conditions caused by problems with junctional proteins
References[edit | edit source]
↑ 1.01.11.21.3Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.
↑ 2.02.1Protonotarios, Nikos; Tsatsopoulou, Adalena (2006). "Naxos disease: Cardiocutaneous syndrome due to cell adhesion defect". Orphanet Journal of Rare Diseases. 1 (1): 4. doi:10.1186/1750-1172-1-4. PMC 1435994. PMID 16722579.
↑McKoy G, Protonotarios N, Crosby A, et al. (June 2000). "Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)". Lancet. 355 (9221): 2119–24. doi:10.1016/S0140-6736(00)02379-5. PMID 10902626. S2CID 39821701.
↑"Keratoderma with woolly hair". Genetics Home Reference. April 17, 2018. Archived from the original on April 18, 2018. Retrieved April 17, 2018.
↑"Naxos disease | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2021-03-18. Retrieved 2021-04-04.
↑ 6.06.16.2RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Naxos disease". www.orpha.net. Archived from the original on 21 November 2017. Retrieved 22 August 2021.
External links[edit | edit source]
Classification
OMIM: 601214
v
t
e
Cytoskeletal defects
Microfilaments
Myofilament
Actin
Hypertrophic cardiomyopathy 11
Dilated cardiomyopathy 1AA
DFNA20
Nemaline myopathy 3
Myosin
Elejalde syndrome
Hypertrophic cardiomyopathy 1, 8, 10
Usher syndrome 1B
Freeman–Sheldon syndrome
DFN A3, 4, 11, 17, 22; B2, 30, 37, 48
May–Hegglin anomaly
Troponin
Hypertrophic cardiomyopathy 7, 2
Nemaline myopathy 4, 5
Tropomyosin
Hypertrophic cardiomyopathy 3
Nemaline myopathy 1
Titin
Hypertrophic cardiomyopathy 9
Other
Fibrillin
Marfan syndrome
Weill–Marchesani syndrome
Filamin
FG syndrome 2
Boomerang dysplasia
Larsen syndrome
Terminal osseous dysplasia with pigmentary defects