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Vascular Ehlers-Danlos syndrome: A null COL3A1 variant found in a patient with loin pain without marked cutaneous
Shreenidhi Ranganatha Subramaniam1,2, Lam Fung Yeung3, L Y Lois Choy1,2
1Department of Chemical Pathology Prince of Wales Hospital, Hospital Authority Hong Kong China.
Abstract:
Patients with null variants may have milder vascular Ehlers-Danlos syndrome, presenting with seemingly non-specific complaints and subtle cutaneous features that may be missed. A high index of suspicion and early genetic testing (aided by next-generation sequencing) were crucial for prevention of life-threatening complications in the patient and family members.
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