- Klippel–
Trénaunay syndrome,
formerly Klippel–
Trénaunay–Weber
syndrome and
sometimes angioosteohypertrophy syndrome and
hemangiectatic hypertrophy, is a...
-
stains may be part of a
syndrome such as Sturge–Weber
syndrome or Klippel–
Trénaunay–Weber syndrome.
Nevus flammeus may be
divided as follows:
Nevus flammeus...
-
birth defects Pretibial myxedema Other diseases, such as the rare Klippel–
Trénaunay syndrome, can
initially be
misdiagnosed as elephantiasis. "Definition...
-
sporadic as most
cases often are. PWS is
often confused with Klippel–
Trénaunay syndrome (KTS).
These two
diseases are similar, but they are distinct...
-
expanded to
include individuals with
capillary vascular birthmarks,
Klippel Trenaunay (KT) and Port Wine Birthmarks.[citation needed] Sturge-Weber Syndrome...
-
condition in 1863. It is
unrelated to Sturge–Weber syndrome, Klippel–
Trénaunay–Weber
syndrome or Osler–Weber–Rendu syndrome.
These conditions are named...
-
lipomatosa Fibrolipomatous hamartoma Neurofibromatosis type 1 Klippel–
Trénaunay syndrome Parkes Weber syndrome Sotos syndrome Hemangiomas Many sources...
-
differential diagnosis.
Children with some
overgrowth syndromes such as Klippel–
Trénaunay syndrome can be
readily detectable at birth. In contrast,
other overgrowth...
- lymphedema,
including Turner syndrome, Milroy's disease, and Klippel–
Trénaunay syndrome. In
these syndromes it may
occur as a
result of
absent or malformed...
-
Proteus syndrome Macrodystrophia lipomatosa[citation needed] Klippel–
Trénaunay syndrome[citation needed]
Parkes Weber syndrome[citation needed] Surgical...
