Klippel-Trenaunay-Weber syndrome is characterized by limb hypertrophy, varicose veins, and vascular nevus. The orofacial manifestations include early eruption of permanent teeth and hemifacial hypertrophy. This 5-year-old male patient had facial asymmetry, limb abnormalities, and a thumb-sucking habit. Cephalometric analysis revealed a Class II open bite occlusion. (Pediatr Dent 16:231-35, 1994)

Klippel Trenaunay syndrome is a rare mixed vascular malformation characterized by a triad of port wine stain, varicose veins, and bony, soft tissue hypertrophy involving an extremity [1]. A rare case involving face and all the limbs is being reported. This is a case of interest also because of having clinical overlap with Proteus syndrome.

Müllerian-duct aplasia, renal agenesis, and cervical somite dysplasia (MURCS) is a rare genetic disorder. Previously thought to be exclusive in females, there have now been a small number of case reports describing a male analogue. We describe a patient with obstructive azoospermia and Klippel-Feil anomaly.

We present a rare case of Stewart-Treves syndrome characterized by a diffuse angiosarcoma of the leg in a 22-year-old man with a history of chronic lymphedema due to Klippel-Trénaunay-Weber syndrome. He underwent limb disarticulation and medical treatment with cycles of doxorubicin, oral thalidomide and sunitinib with a very good response after 12 months of follow-up.

We would like to present a case of Klippel-Feil Syndrome in which it is associated with multiple cervical vertebra synostosis, short neck, cervical rib, congenital sclerosis, platybasia, spina-bifida and deafness. We are revising the case history of this syndrome.

A 24-year-old man with a history of Klippel-Trenaunay-Weber syndrome presented with severe headache and neck pain. Work-up revealed subarachnoid hemorrhage and evidence of multiple intracranial aneurysms. The patient was treated with open surgical clipping of his ruptured aneurysm and is currently doing well.

We describe two patients with associations of hereditary neuropathies and heritable skeletal disorders not previously reported. The first patient had Marfan's syndrome and hereditary motor and sensory neuropathy Type 1. The second patient had Ehlers-Danlos syndrome, Klippel-Feil syndrome and tomaculous neuropathy.

Klippel-Trénaunay syndrome is a rare congenital syndrome characterized by capillary malformations, soft tissue and bone hypertrophy, and varicose veins. There is a well-established risk for thrombotic complications in these patients. A case of a young patient diagnosed post partum with the very rare liver involvement is presented. The complex clinical course, the multidisciplinary management an...

A 44-year-old man with no relevant past medical history was referred for colonoscopy because of recurrent hematochezia and iron deficiency anemia. He reported no abdominal pain or weight loss. He had been on oral therapy with ferrous sulfate. A hypertrophic lower left limb was seen on physical examination. Colonoscopy (●" Video1) revealed ectasia and congestion of the submucosal and mucosal ves...

109 Anesthetic Considerations in a Parturient with a Klippel-Trenaunay Weber Syndrome Abstract Type: Case Report/Case Series Alaa A. Abd-Elsayed, M.D., M.P.H.; Joseph Baus, M.D.; Thomas James, M.D. University of CincinnatiType: Case Report/Case Series Alaa A. Abd-Elsayed, M.D., M.P.H.; Joseph Baus, M.D.; Thomas James, M.D. University of Cincinnat