Hi! So let's learn EDS together. I've tabled a list of high-yield points of all the types of EDS. It requires little bit of revision but once you get a pictorial familiarity you should be able to recall them all.
Have fun!
- They are all Autosomal Dominant.
- They have common Clinical features - skin HYPERelasticity, joint HYPERmobility and HYPER (easy) bruising.
- Go serially, Classical has the first 2, Type I and II and HYPERmobile is III and lastly Vascular is type IV
- Vascular type has additionally - arterial & uterine rupture.
- EDS types with enzyme defects are Autosomal Recessive. So, 4 and 6 are AR.
- Kyphoscoliotic EDS is Type VI (K rearranged is a V and I)
- For the last 2, mnemonic is ABCDð Arthrochalasia VII a, b and VII c is Dermatosparaxis.
- KyphoSCOLIOTIC EDS - defective lysyl hydroxylase (=> abnormal cross linking of collagen or KOLLAGEN => think of bones ðĶī => congenital SCOLIOSIS)
- ARTHROchalasia is COL IA (1st letter is A) and hence presents with severe JOINT hyper mobility.
- DERMATospARaxis is AR and a defective Procollagen-N-peptidase and presents with CUTIS laxa. (Cuties are Pros ;)
