Legius syndrome (LS) is an autosomal dominant condition characterized by cafe au lait spots. It was first described in 2007 and is often mistaken for...

2017. Legius E, Stevenson D (2015). Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Gripp KW, Mirzaa GM, Amemiya A (eds.). Legius Syndrome. Seattle...

Leaky gut syndrome Legg–Calvé–Perthes disease Legius syndrome Leiner's disease Lelis syndrome Lemierre's syndrome Lennox–Gastaut syndrome Lenz microphthalmia...

recent years, in the past NF-1 was in some cases confused with Legius syndrome, another syndrome with vaguely similar symptoms, including cafe-au-lait spots...

hypomelanosis Joubert syndrome Keipert syndrome Legius syndrome LEOPARD syndrome Lethal congenital contracture syndrome MASA syndrome Megalencephaly, autosomal...

polydactyly are: Bardet–Biedl syndrome, Meckel syndrome, Pallister–Hall syndrome, Legius syndrome, Holt–Oram syndrome. Central polydactyly can also be...

occurs in other disease processes that closely resemble NF1, such as Legius syndrome (cafe-au-lait spots, axillary freckling, and macrocephaly without Lisch...

malformation syndrome (CV-AVM) Cardiofaciocutaneous syndrome (CFC) Neurofibromatosis type I (NF1) Noonan syndrome (NS) Costello syndrome (CS) Legius syndrome, also...

meningocele syndrome Legius syndrome Lethal congenital contracture syndrome 1, 2, 7, and 9 Lethal Kniest-like syndrome Lethal multiple pterygium syndrome Lissencephaly...

Hippel-Lindau syndrome and Legius syndrome are inherited in an autosomal dominant manner. Incontinentia pigmenti is X-linked dominant and Sturge-Weber syndrome is...