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* This file is copyright 2017 State of the Netherlands (Ministry of Interior Affairs and Kingdom Relations).
* It is made available under the terms of the GNU Affero General Public License, version 3 as published by the Free Software Foundation.
* The project of which this file is part, may be found at
*/

package nl.bzk.brp.model.data.autaut;

import org.springframework.roo.addon.dbre.RooDbManaged;
import org.springframework.roo.addon.javabean.RooJavaBean;
import org.springframework.roo.addon.jpa.activerecord.RooJpaActiveRecord;
import org.springframework.roo.addon.tostring.RooToString;

@RooJavaBean
@RooToString
@RooJpaActiveRecord(versionField = “”, table = “autaut”, schema = “autaut”)
@RooDbManaged(automaticallyDelete = true)
public class Autaut {
}
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The term juvenile localized scleroderma (JLS) covers a subgroup of scleroderma that is recognized to occur in children as young as 2 years old. There are several clinical subtypes of JLS, including the linear scleroderma, kedem-like sclerosis, undifferentiated scleroderma, and craniofacial scleroderma. The linear scleroderma variant is the most common variant and can be localized to the head and neck, trunk, distal extremities, or limbs. The kedem-like sclerosis subtype of JLS is characterized by white markings on the trunk and extremities and is clinically similar to Juvenile Dermatomyositis. The undifferentiated scleroderma subtype of JLS is typified by the loss of all skeletal muscle tone and can lead to paralysis, limb contractures, and involvement of the oesophagus. Craniofacial scleroderma involves ocular, oral, and facial tissues and is characterized by eyelid retraction and often enophthalmos. Diagnostic criteria for JLS include arthritis, marked joint contractures, and other evidence of scleroderma such as Raynaud’s phenomenon, calcinosis, and marked digital
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