Fever, and Psoriasiform dermatitis

Diseases related with Fever and Psoriasiform dermatitis

In the following list you will find some of the most common rare diseases related to Fever and Psoriasiform dermatitis that can help you solving undiagnosed cases.

Top matches:

Related symptoms:

  • Fever
  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Ichthyosis


SOURCES: OMIM MENDELIAN

More info about PSORIASIS 2; PSORS2

Psoriasis (psoriasis vulgaris; PV) is a chronic inflammatory dermatosis that affects approximately 2% of the population. It is characterized by red, scaly skin patches that are usually found on the scalp, elbows, and knees, and may be associated with severe arthritis. The lesions are caused by abnormal keratinocyte proliferation and infiltration of inflammatory cells into the dermis and epidermis. The usual age of onset of psoriasis is between 15 and 30 years, although it can present at any age (summary by Matthews et al., 1996).Generalized pustular psoriasis (GPP) is a life-threatening disease characterized by sudden, repeated episodes of high-grade fever, generalized rash, and disseminated pustules, with hyperleukocytosis and elevated serum levels of C-reactive protein (OMIM ) (summary by Marrakchi et al., 2011). GPP often presents in patients with existing or prior psoriasis vulgaris; however, GPP can develop without a history of PV (Sugiura et al., 2013). Palmoplantar pustulosis and acrodermatitis continua of Hallopeau represent acral forms of pustular psoriasis that have historically been grouped with GPP (summary by Setta-Kaffetzi et al., 2013).Nestle et al. (2009) provided a detailed review of the pathogenesis and genetics of psoriasis. Genetic Heterogeneity of Psoriasis and Psoriasis SusceptibilityPSORS2 (OMIM ) is caused by mutation in the CARD14 gene (OMIM ) on chromosome 17q25, and PSORS14 (OMIM ) is caused by mutation in the IL36RN gene (OMIM ) on chromosome 2q14.Psoriasis susceptibility loci include PSORS1 on 6p21.3; PSORS3 (OMIM ) on 4q; PSORS4 on 1q21; PSORS5 (OMIM ) on 3q21; PSORS6 (OMIM ) on 19p; PSORS7 (OMIM ) on 1p; PSORS8 (OMIM ) on 16q; PSORS9 (OMIM ) on 4q31; PSORS10 (OMIM ) on 18p11; PSORS11 (OMIM ) on 5q31-q33; PSORS12 (OMIM ) on 20q13; PSORS13 (OMIM ), conferred by variation in the TRAF3IP2 gene (OMIM ) on 6q21; and PSORS15 (OMIM ), conferred by variation in the AP1S3 gene (OMIM ) on 2q36.An additional putative psoriasis candidate locus has been reported on 20p (Nair et al., 1997).

Related symptoms:

  • Fever
  • Arthritis
  • Skin rash
  • Scaling skin
  • Psoriasiform dermatitis


SOURCES: OMIM MENDELIAN

More info about PSORIASIS 1, SUSCEPTIBILITY TO; PSORS1

MAJEED SYNDROME; MJDS Is also known as chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and neutrophilic dermatosis

Related symptoms:

  • Growth delay
  • Anemia
  • Flexion contracture
  • Fever
  • Delayed skeletal maturation


SOURCES: OMIM MENDELIAN

More info about MAJEED SYNDROME; MJDS

Other less relevant matches:

Generalized pustular psoriasis is a severe inflammatory skin disease that can be life-threatening and that is characterized by recurrent episodes of high fever, fatigue, episodic erythematous cutaneous eruptions with sterile cutaneous pustules formation on various parts of the body, and neutrophil leukocytosis.

GENERALIZED PUSTULAR PSORIASIS Is also known as ditra|interleukin 36 receptor antagonist deficiency|acrodermatitis continua of hallopeau|generalized pustular psoriasis|psorp|gpp|palmoplantar pustulosis

Related symptoms:

  • Muscle weakness
  • Fever
  • Headache
  • Erythema
  • Skin rash


SOURCES: OMIM ORPHANET MENDELIAN

More info about GENERALIZED PUSTULAR PSORIASIS

Sterile multifocal osteomyelitis with periostitis and pustulosis is a rare, severe, genetic autoinflammatory syndrome characterized by usually neonatal onset of generalized neutrophilic cutaneous pustulosis and severe, recurrent, multifocal, aseptic osteomyelitis with marked periostitis, typically affecting distal ribs, long bones and vertebral bodies. High levels of acute-phase reactants (with no fever associated) and onychosis are frequently observed additional features.

STERILE MULTIFOCAL OSTEOMYELITIS WITH PERIOSTITIS AND PUSTULOSIS Is also known as interleukin-1 receptor antagonist deficiency|interleukin 1 receptor antagonist deficiency|autoinflammatory disease due to interleukin-1 receptor antagonist deficiency|dira|ompp

Related symptoms:

  • Pain
  • Feeding difficulties
  • Hepatomegaly
  • Fever
  • Respiratory insufficiency


SOURCES: ORPHANET OMIM MENDELIAN

More info about STERILE MULTIFOCAL OSTEOMYELITIS WITH PERIOSTITIS AND PUSTULOSIS

Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.

TAKAYASU ARTERITIS Is also known as young female arteritis|aortic arch syndrome|pulseless disease

Related symptoms:

  • Seizures
  • Muscle weakness
  • Anemia
  • Hypertension
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about TAKAYASU ARTERITIS

Netherton syndrome (NS) is a skin disorder characterized by congenital ichthyosiform erythroderma (CIE), a distinctive hair shaft defect (trichorrhexis invaginata; TI) and atopic manifestations.

NETHERTON SYNDROME Is also known as erythroderma, ichthyosiform, with hypotrichosis and hyper-ige|comÈl-netherton syndrome|bamboo hair syndrome|comel-netherton syndrome|ns|netherton disease

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Growth delay


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about NETHERTON SYNDROME

VELOCARDIOFACIAL SYNDROME Is also known as chromosome 22q11.2 deletion syndrome|shprintzen vcf syndrome|vcf syndrome|vcfs

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about VELOCARDIOFACIAL SYNDROME

DiGeorge syndrome (DGS) comprises hypocalcemia arising from parathyroid hypoplasia, thymic hypoplasia, and outflow tract defects of the heart. Disturbance of cervical neural crest migration into the derivatives of the pharyngeal arches and pouches can account for the phenotype. Most cases result from a deletion of chromosome 22q11.2 (the DiGeorge syndrome chromosome region, or DGCR). Several genes are lost including the putative transcription factor TUPLE1 which is expressed in the appropriate distribution. This deletion may present with a variety of phenotypes: Shprintzen, or velocardiofacial, syndrome (VCFS ); conotruncal anomaly face (or Takao syndrome); and isolated outflow tract defects of the heart including tetralogy of Fallot, truncus arteriosus, and interrupted aortic arch. A collective acronym CATCH22 has been proposed for these differing presentations. A small number of cases of DGS have defects in other chromosomes, notably 10p13 (see {601362}). In the mouse, a transgenic Hox A3 (Hox 1.5) knockout produces a phenotype similar to DGS as do the teratogens retinoic acid and alcohol.

DIGEORGE SYNDROME; DGS Is also known as hypoplasia of thymus and parathyroids|chromosome 22q11.2 deletion syndrome|third and fourth pharyngeal pouch syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: OMIM MENDELIAN

More info about DIGEORGE SYNDROME; DGS

High match H SYNDROME

H syndrome is a systemic inherited histiocytosis, with characteristic cutaneous findings accompanying systemic manifestations. H syndrome refers to the major clinical findings of hyperpigmentation, hypertrichosis, hepatosplenomegaly, heart anomalies, hearing loss, hypogonadism, low height, and occasionally, hyperglycemia/diabetes mellitus. Due to overlapping clinical features, H syndrome is now considered to include pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (PHID), Faisalabad histiocytosis (FHC) and familial sinus histiocytosis with massive lymphadenopathy (FSHML).

H SYNDROME Is also known as sinus histiocytosis and massive lymphadenopathy|hjcd|shml|hyperpigmentation, cutaneous, with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss|h syndrome|faisalabad histiocytosis|pigmented hypertrichosis wi

Related symptoms:

  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Growth delay


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about H SYNDROME

Top 5 symptoms//phenotypes associated to Fever and Psoriasiform dermatitis

Symptoms // Phenotype % cases
Arthritis Uncommon - Between 30% and 50% cases
Anemia Uncommon - Between 30% and 50% cases
Skin rash Uncommon - Between 30% and 50% cases
Short stature Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Fever and Psoriasiform dermatitis. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Global developmental delay Scaling skin Arthralgia Epidermal acanthosis Inflammatory abnormality of the skin Posteriorly rotated ears Hyperkeratosis Amenorrhea Ichthyosis Hypothyroidism Patent ductus arteriosus Abnormal heart morphology Leukocytosis Atrial septal defect Hydrocephalus Ventricular septal defect Hearing impairment Recurrent infections Intellectual disability Primary amenorrhea Osteomyelitis Rheumatoid arthritis Growth delay Flexion contracture Pustule

Rare Symptoms - Less than 30% cases

Arteria lusoria Immunodeficiency Abnormality of cardiovascular system morphology Thrombocytopenia Hernia Obesity Conotruncal defect Aplasia of the thymus Inguinal hernia Retinal vascular tortuosity Retrognathia Umbilical hernia Conductive hearing impairment Behavioral abnormality Hypoplasia of the corpus callosum Right aortic arch with mirror image branching Microcephaly Failure to thrive Ptosis Alopecia Hydronephrosis Malabsorption Generalized hypotonia Hypertelorism Scoliosis Blepharophimosis Abnormal facial shape Cleft palate Cognitive impairment High palate Delayed speech and language development Sacral meningocele Short neck Abnormality of the pinna Autoimmunity Perimembranous ventricular septal defect Hypoparathyroidism Autoimmune hemolytic anemia Autoimmune thrombocytopenia Right aortic arch Posterior embryotoxon Bipolar affective disorder Vitiligo Meningocele Acne Truncus arteriosus Myelomeningocele Juvenile rheumatoid arthritis Seborrheic dermatitis Aplasia of the uterus Graves disease Interrupted aortic arch Inflammation of the large intestine Unilateral renal agenesis Bulbous nose Abnormality of the kidney Hemolytic anemia Bifid uvula Chorea Renal agenesis Specific learning disability Duodenal stenosis Low posterior hairline Renal dysplasia Cholelithiasis Spina bifida Hypocalcemia Impaired T cell function Bicuspid aortic valve Arnold-Chiari malformation Schizophrenia Nasal speech Purpura Tetralogy of Fallot Palmoplantar pustulosis Weight loss Parakeratosis Sepsis Retinopathy Atopic dermatitis Muscle weakness Chronic recurrent multifocal osteomyelitis Splenomegaly Osteolysis Low-grade fever Vasculitis Periostitis Onychomadesis Hepatomegaly Delayed skeletal maturation Hepatosplenomegaly Microcytic anemia Episodic fever Abnormality of the thymus Femoral hernia Hypoplasia of the thymus Perisylvian polymicrogyria Vascular tortuosity Abnormality of the middle ear Esophoria Accommodative esotropia Decreased circulating parathyroid hormone level Alcoholism Hyperreflexia Parathyroid hypoplasia Ventriculomegaly Severe short stature Pneumonia Clinodactyly Intellectual disability, mild Edema Anteverted nares Frontal bossing Parathyroid agenesis Wide nasal bridge Brachydactyly Tetany Epicanthus Sensorineural hearing impairment Type I truncus arteriosus Anterior segment developmental abnormality Increased inflammatory response Sclerocornea Orthokeratosis Low-set ears Strabismus Micrognathia Neoplasm Unilateral primary pulmonary dysgenesis Unilateral lung agenesis Diffuse skin atrophy Microphthalmia Congenital conductive hearing impairment Perineal fistula Vascular ring Central nervous system degeneration Acute monocytic leukemia Nail pits Hypertonia Narrow mouth Exotropia Polymicrogyria Amblyopia Broad thumb Hypogonadism Coarctation of aorta High, narrow palate Iris coloboma Astigmatism Telecanthus Generalized tonic-clonic seizures Microtia Short philtrum Attention deficit hyperactivity disorder Craniosynostosis Dermal atrophy Cleft lip Short palpebral fissure Micropenis Diabetes mellitus Exocrine pancreatic insufficiency Recurrent pharyngitis Decreased serum testosterone level Communicating hydrocephalus Varicose veins Aspiration pneumonia Abnormal eyebrow morphology Enlarged kidney Severe sensorineural hearing impairment Skin nodule Polycythemia Scleroderma Lipoatrophy Elevated erythrocyte sedimentation rate Increased antibody level in blood Hallux valgus Hyperglycemia Nasal obstruction Histiocytosis Lipodystrophy Panniculitis Retroperitoneal fibrosis Upper eyelid edema Bilateral camptodactyly Cervical lymphadenopathy Stiff skin Snoring Episcleritis Facial telangiectasia Reticulocytopenia Myelofibrosis Generalized lymphadenopathy Corneal arcus Hyperplasia of the maxilla Broad finger Pancreatic hypoplasia Abnormality of cardiovascular system physiology Chronic rhinitis Stridor Sleep apnea Proptosis Delayed puberty Full cheeks Recurrent fractures Polyneuropathy Flat face Cleft upper lip Lymphadenopathy Abnormality of the foot Hypotrichosis Wide intermamillary distance Pectus carinatum Abnormal cardiac septum morphology Apnea Camptodactyly Low-set, posteriorly rotated ears Pes planus Dyspnea Growth hormone deficiency Decreased testicular size Azoospermia Gingival overgrowth Plagiocephaly Type I diabetes mellitus Elbow flexion contracture Hypergonadotropic hypogonadism Aspiration Gynecomastia Hyperpigmentation of the skin Telangiectasia Overgrowth Bronchiectasis Hypertrichosis Hypertriglyceridemia Blue sclerae Epistaxis Cardiomegaly Bilateral sensorineural hearing impairment Mitral valve prolapse Psychotic episodes Platybasia Velopharyngeal insufficiency IgE-mediated food allergy Muscular hypotonia Reduced consciousness/confusion Abnormal aortic valve morphology Inflammatory abnormality of the eye Abnormal pattern of respiration Arterial stenosis Brittle scalp hair Cataract Hypernatremic dehydration Hypernatremia Immunologic hypersensitivity Angioedema Increased IgE level Allergic rhinitis Cerebral ischemia Gangrene Congenital nonbullous ichthyosiform erythroderma Pulmonary arterial hypertension Hypospadias Hypertrophic cardiomyopathy Neurological speech impairment Absent speech Chest pain Migraine Cerebellar atrophy Hemoptysis Intellectual disability, severe Myocardial infarction Subcutaneous nodule Anorexia Skin ulcer Aortic regurgitation Abnormal heart valve morphology Trichorrhexis nodosa Allergy Myalgia Asthma Sparse and thin eyebrow Sparse scalp hair Fine hair Eczema Dehydration Decreased antibody level in blood Dry skin Aminoaciduria Ascending tubular aorta aneurysm Pruritus Abnormal endocardium morphology Recurrent respiratory infections Amaurosis fugax Gastrointestinal infarctions Arteritis Abnormality of the hair Sparse eyelashes Verrucae Ectopic kidney Villous atrophy Hypothermia Severe postnatal growth retardation Irregular hyperpigmentation Congenital ichthyosiform erythroderma Abnormality of the musculature Malnutrition Acanthosis nigricans Emphysema Erythroderma Intracranial hemorrhage Brittle hair Urticaria Recurrent skin infections Abnormal intestine morphology Depressivity Hyperhidrosis Giant platelets Myopathic facies Furrowed tongue Submucous cleft hard palate Axonal loss Cholangitis Basal ganglia calcification Abnormality of the ear Chills Nail dysplasia Hypoplasia of the brainstem Neutrophilia Asthenia Obsessive-compulsive behavior Apathy Dysdiadochokinesis Geographic tongue Anal stenosis Nausea Oligoarthritis Congenital hypoplastic anemia Paranoia Bone pain Mood swings Hypertensive crisis Anemia of inadequate production Decreased mean corpuscular volume Pulmonary artery atresia Nail dystrophy Abnormality of the endocrine system Echolalia Pierre-Robin sequence Delusions Headache Hearing abnormality Erythema Abnormality of the hand Pain Dementia Mental deterioration Anal atresia Pulmonic stenosis Congenital cataract Thrombocytosis Stomatitis Fused cervical vertebrae Aggressive behavior Joint swelling Anxiety Fetal distress Cerebral vasculitis Hypertension Fatigue Hyperactivity Dilatation Dysmetria Fragile skin Feeding difficulties Open mouth Holoprosencephaly Narrow palpebral fissure Multicystic kidney dysplasia Respiratory insufficiency Respiratory distress Hallucinations Osteopenia Vertebral fusion Psychosis Meningitis Peripheral demyelination Hyperostosis Underdeveloped nasal alae Vesicoureteral reflux Interstitial pulmonary abnormality Seborrheic keratosis


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