About: Neonatal-onset multisystem inflammatory disease

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Neonatal-onset multisystem inflammatory disease is a rare genetic periodic fever syndrome which causes uncontrolled inflammation in multiple parts of the body starting in the newborn period. Symptoms include skin rashes, severe arthritis, and chronic meningitis leading to neurologic damage. It is one of the cryopyrin-associated periodic syndromes. This syndrome is also known as the Prieur–Griscelli syndrome as it was first described by these authors in 1981.

Attributes	Values
rdf:type	Thing Disease disease
rdfs:label	المرض الالتهابي متعدد الأجهزة وليدي البدء (ar) Síndrome de CINCA (ca) Enfermedad inflamatoria sistémica de inicio neonatal (es) Syndrome cinca (fr) Neonatal-onset multisystem inflammatory disease (en)
rdfs:comment	المتلازمة الجلدية والمفصلية العصبية الطفولية المزمنة (بالإنجليزية: Chronic infantile neurologic cutaneous and articular syndrome ومختصرها CINCA)‏ أو المرض الالتهابي متعدد الأجهزة وليدي البدء (بالإنجليزية: Neonatal onset multisystem inflammatory disease ومختصرها NOMID)‏ أو متلازمة برير-غريسيلي (بالإنجليزية: Prieur-Griscelli syndrome)‏ أو متلازمة أنسل-بايواترز-إلدركنغ (بالإنجليزية: Ansell-Bywaters-Elderking syndrome)‏ هي متلازمة حمى دورية وراثية نادرة تتسبب بالتهاب غير مسيطر عليه في أجزاء مختلفة من الجسم وتبدأ بعد فترة قصيرة من الولادة. (ar) Le syndrome CINCA (acronyme de Chronique, Infantile, Neurologique, Cutané, Articulaire ) est une maladie génétique rare (maladie auto-inflammatoire) qui toucherait une centaine d'enfants dans le monde.Sa désignation anglophone est NOMID (pour Neonatal Onset Multisystem Inflammatory Disease). (fr) La síndrome de CINCA, síndrome de NOMID o malaltia inflamatòria sistèmica d'inici neonatal,és una malaltia d'origen genètic i transmissió autosòmica dominant que s'inclou dins del grup de trastorns anomenats síndromes diaris associats a criopirina . Aquest grup de malalties genètiques presenten mutacions localitzades en el cromosoma 1 humà, en el gen CIAS1 que codifica la proteïna criopirina . (ca) La enfermedad inflamatoria sistémica de inicio neonatal, conocida también como síndrome CINCA por las iniciales de su nombre en inglés (chronic infantile neurologic, cutaneous and articular) o NOMID (neonatal-onset multisystem inflammatory disease), es una enfermedad de origen genético y transmisión autosómica dominante que se incluye dentro del grupo de trastornos llamados síndromes periódicos asociados a criopirina. Este grupo de enfermedades genéticas presentan mutaciones localizadas en el cromosoma 1 humano, en el gen CIAS1 que codifica la proteína . (es) Neonatal-onset multisystem inflammatory disease is a rare genetic periodic fever syndrome which causes uncontrolled inflammation in multiple parts of the body starting in the newborn period. Symptoms include skin rashes, severe arthritis, and chronic meningitis leading to neurologic damage. It is one of the cryopyrin-associated periodic syndromes. This syndrome is also known as the Prieur–Griscelli syndrome as it was first described by these authors in 1981. (en)
foaf:name	Neonatal-onset multisystem inflammatory disease (en)
name	Neonatal-onset multisystem inflammatory disease (en)
dcterms:subject	Rheumatology Rare diseases Neonatology
Wikipage page ID	6364856 (xsd:integer)
Wikipage revision ID	1101412244 (xsd:integer)
Link from a Wikipage to another Wikipage	Canakinumab Puberty Elbow Muckle–Wells syndrome Meninges Mevalonate kinase Deficiency of the interleukin-1–receptor antagonist Ankle Rheumatology Hydrocephalus Hypertrophic Patella Uveitis Infant Spleen Amyloid Amyloidosis Meningitis Rare disease Colchicine Eosinophil Granulocytes Brain Conjunctivitis Cryopyrin-associated periodic syndrome Marshall syndrome Anemia Liver Lymph node Macrocephaly Cerebral atrophy Aicardi–Goutières syndrome Castleman's disease Joint Juvenile idiopathic arthritis Anakinra Erythrocyte sedimentation rate Familial Mediterranean fever Amenorrhoea Central nervous system Fontanelle Granulocyte Rare diseases Hyperimmunoglobulin D syndrome Arthritis Neonatology Wrist dbr:C-reactive_protein dbr:Methotrexate Neopterin Cartilage Seizures Knee Schnitzler syndrome Skin Ultrasound Umbilical cord Eye Ventriculomegaly Periodic fever syndrome Placenta Sensorineural hearing loss Sequelae Urticaria List of cutaneous conditions Epiphyses Vasculature Familial cold urticaria Optic atrophy Contractures CD10 CIAS1
sameAs	Neonatal-onset multisystem inflammatory disease Neonatal-onset multisystem inflammatory disease Neonatal-onset multisystem inflammatory disease Neonatal-onset multisystem inflammatory disease Neonatal-onset multisystem inflammatory disease Neonatal-onset multisystem inflammatory disease Neonatal-onset multisystem inflammatory disease
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