Sneddon syndrome associated with Protein S deficiency.

[sneddon syndrome]

Sneddon syndrome (SS ) is rare , arterio-occlusive disorder characterized by generalized livedo racemosa of the skin and various central nervous symptoms due to occlusion of medium-sized arteries of unknown . Seizure , cognitive impairment , hypertension , and history of repetitive miscarriages are the other symptoms seen in this disease . Livedo racemosa involves persisting irreversible skin lesions red or blue in color with irregular margins . Usually , SS occurs in women of childbearing age . Protein S deficiency is an inherited or acquired disorder associated with an increased risk of thrombosis . We present a 33 -year -old woman with SS with diffuse livedo racemosa , recurrent cerebrovascular diseases , migraine -type headache , sinus vein thrombosis , and protein S deficiency . Protein S deficiency and with Sneddon syndrome rarely encountered in the literature .

Diseases
Validation

Diseases presenting "hypertension" symptom

achondroplasia

acute rheumatic fever

adrenal incidentaloma

aniridia

aromatase deficiency

cadasil

child syndrome

cohen syndrome

congenital adrenal hyperplasia

congenital diaphragmatic hernia

cushing syndrome

cystinuria

erdheim-chester disease

erythropoietic protoporphyria

esophageal adenocarcinoma

fabry disease

familial hypocalciuric hypercalcemia

gm1 gangliosidosis

heparin-induced thrombocytopenia

hereditary cerebral hemorrhage with amyloidosis

holt-oram syndrome

homocystinuria without methylmalonic aciduria

hydrocephalus with stenosis of the aqueduct of sylvius

inclusion body myositis

kallmann syndrome

kindler syndrome

lamellar ichthyosis

lymphangioleiomyomatosis

pendred syndrome

primary effusion lymphoma

scrub typhus

severe combined immunodeficiency

sneddon syndrome

typhoid

von hippel-lindau disease

well-differentiated liposarcoma

werner syndrome

x-linked adrenoleukodystrophy

zellweger syndrome

This symptom has already been validated