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CHST14 EDS/musculocontractural EDS The features of this rare condition (MIM 601776) include progressive kyphoscoliosis, adducted thumbs in infancy, clubfoot, arachnodactyly, joint hypermobility, fragile and hyperextensible skin with atrophic scars and delayed wound healing.20 22 Arthrochalasic EDS Arthrochalasic EDS (MIM 130060) is extremely rare.23 Congenital bilateral hip dislocation, severe joint hypermobility with recurrent dislocations, skin hyperextensibility, easy bruising, atrophic scars, kyphoscoliosis and osteopaenia are the features of this autosomal-dominant condition

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7 Discussion Current MASLD management primarily relies on lifestyle interventions, including weight reduction, dietary modification, and physical activity (86, 87)

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The Journal of Physiology , 589(Pt 4), 963-973

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