»	Dermal Disorders
	»	Osteogenesis Imperfecta (OI)
	»	Ehlers–Danlos Syndrome
	»	Marfan Syndrome
	»	Pseudoxanthoma Elasticum (PXE)
	»	Cutis Laxa
	»	Congenital Contractural Arachnodactyly
	»	Focal Dermal Hypoplasia (Goltz Syndrome)
	»	Berardinelli–Seip Congenital Lipodystrophy
	»	Familial Partial Lipodystrophy
	»	Buschke–Ollendorf Syndrome
	»	Lipoid Proteinosis (Urbache–Wiethe Disease)
	»	Beare-Stevenson Cutis Gyrata Syndrome

Cutis Laxa

AR, FBLN5 gene, fibulin 5, AD (elastin gene and FBLN5), XLR (ATP7A gene)
Presents with loose, pendulous skin (inelastic), arterial rupture, lung abnormalities, visceral diverticulae/hernia, joint dislocation, pulmonary emphysema (AR inheritance), newborn with hypoplastic lungs
Acquired form: Marshall syndrome