Correspondence
Histopathological characterisation of molluscoid pseudotumour seen in Ehlers–Danlos syndrome
Saira Agarwala,
Saira Agarwala
Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA
Search for more papers by this author Farhaan Hafeez,
Farhaan Hafeez
Department of Dermatology, St Luke’s University Health System, Temple School of Medicine, Bethlehem, PA, USA
Search for more papers by this author
Saira Agarwala,
Saira Agarwala
Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA
Search for more papers by this author Farhaan Hafeez,
Farhaan Hafeez
Department of Dermatology, St Luke’s University Health System, Temple School of Medicine, Bethlehem, PA, USA
Search for more papers by this author
First published: 13 April 2021
No abstract is available for this article.
Conflicts of interest
The authors state that they have no conflicts of interest.
References
- 1Myllyharju J, Kivirikko KI. Collagens and collagen-related diseases. Ann. Med. 2001; 33; 7–21.
- 2Bowen JM, Sobey GJ, Burrows NP et al. Ehlers-Danlos syndrome, classical type. Am. J. Med. Genet. C Semin. Med. Genet. 2017; 175; 27–39.
- 3Malfait F, Francomano C, Byers P et al. The 2017 international classification of the Ehlers-Danlos syndromes. Am. J. Med. Genet. C Semin. Med. Genet. 2017; 175; 8–26.
- 4Sulica VI, Cooper PH, Pope FM, Hambrick GW Jr, Gerson BM, McKusick VA. Cutaneous histologic features in Ehlers-Danlos syndrome: study of 21 patients. Arch. Dermatol. 1979; 115; 40–42.
