Ehlers-Danlos syndrome- a not so rare entity

Authors

  • Asher Ahmed Mashhood

Keywords:

Ehlers-Danlos syndrome

Abstract

The patient was a young girl who presented with 5 years history of excessive joint mobility,difficulty in wound healing and formation of thin scars over the extensor aspects of the limbs.There was no history of any bleeding tendency, joint subluxation or eye complaints. Onexamination, the skin was soft and hyperextensible and the joints exhibited a great range ofmobility. There were multiple paper-thin scars over the extensor aspects of elbows, knees andshins. There was a ‘molluscoid pseudotumour’ over her right elbow. The patient wasdiagnosed as a case of EDS type I on the basis of history and clinical examination. Thetumour was excised and the histopathology report was consistent with the diagnosis ofmolluscoid pseudotumour. She was prescribed Tab Vitamin C 500mg daily. The patient andthe parents were explained about the disease, its prognosis and complications.

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Published

2017-01-03

How to Cite

1.
Mashhood AA. Ehlers-Danlos syndrome- a not so rare entity. J Pak Assoc Dermatol [Internet]. 2017Jan.3 [cited 2026Feb.26];14(4):248-52. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/831

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