1naresh
Array ( [urn:ac.highwire.org:guest:identity] => Array ( [runtime-id] => urn:ac.highwire.org:guest:identity [type] => guest [service-id] => ajnr-ac.highwire.org [access-type] => Controlled [privilege] => Array ( [urn:ac.highwire.org:guest:privilege] => Array ( [runtime-id] => urn:ac.highwire.org:guest:privilege [type] => privilege-set [privilege-set] => GUEST ) ) [credentials] => Array ( [method] => guest ) ) ) 1nareshArray ( [urn:ac.highwire.org:guest:identity] => Array ( [runtime-id] => urn:ac.highwire.org:guest:identity [type] => guest [service-id] => ajnr-ac.highwire.org [access-type] => Controlled [privilege] => Array ( [urn:ac.highwire.org:guest:privilege] => Array ( [runtime-id] => urn:ac.highwire.org:guest:privilege [type] => privilege-set [privilege-set] => GUEST ) ) [credentials] => Array ( [method] => guest ) ) )Comparison between KTS and Parkes-Weber Syndrome3
KTS Parkes-Weber Syndrome Cutaneous vascular malformation Almost invariably tends to be dark; may be verrucous Frequent; usually a pink capillary malformation Arteriovenous fistulas Not significant Invariablea Deep vein Commona Absent Lateral venous anomaly Commona Absent Gigantism Usually disproportionate with soft-tissue thickening predominating; often giant toes present Usually proportionate Lengthening of limb Usually minor Often minor Associated lesions Common Rare Lymphatics Often hypoplastic Usually hyperplastic Prognosis Good; stable after childhood May be progressive deterioration
a Indicates signs present in our case.