Arthritis, and Psoriasiform dermatitis

Diseases related with Arthritis and Psoriasiform dermatitis

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


Top matches:

Medium match PSORIASIS-RELATED JUVENILE IDIOPATHIC ARTHRITIS


Juvenile psoriatic arthritis is a relatively rare form of juvenile idiopathic arthritis (JIA) representing less than 10% of all JIA cases.

PSORIASIS-RELATED JUVENILE IDIOPATHIC ARTHRITIS Is also known as psoriasis-related jia|juvenile psoriatic arthritis

Related symptoms:

  • Arthritis
  • Autoimmunity
  • Inflammatory abnormality of the skin
  • Psoriasiform dermatitis
  • Juvenile rheumatoid arthritis


SOURCES: OMIM ORPHANET MENDELIAN

More info about PSORIASIS-RELATED JUVENILE IDIOPATHIC ARTHRITIS

Medium match SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS


Seborrhea-like dermatitis with psoriasiform elements is a rare, genetic, epidermal disorder characterized by a chronic, diffuse, fine, scaly erythematous rash on the face (predominantly the chin, nasolabial folds, eyebrows), around the earlobes and over the scalp, associated with hyperkeratosis over elbows, knees, palms, soles and metacarpophalangeal joints, in the absence of associated rheumatological or neurological disorders. Cold weather, emotional stress and strenuous physical activity may exacerbate symptoms.

Related symptoms:

  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Skin rash
  • Overgrowth


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS

Medium match PSORIASIS 2; PSORS2


Related symptoms:

  • Fever
  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Ichthyosis


SOURCES: OMIM MENDELIAN

More info about PSORIASIS 2; PSORS2

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Other less relevant matches:

Medium match PSORIASIS 1, SUSCEPTIBILITY TO; PSORS1


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

Medium match SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1; SPDA1


Spondyloarthropathy (SpA), one of the commonest chronic rheumatic diseases, includes a spectrum of related disorders comprising the prototype ankylosing spondylitis (AS), a subset of psoriatic arthritis (PsA), reactive arthritis (ReA), arthritis associated with inflammatory bowel disease, and undifferentiated spondyloarthropathy (Miceli-Richard et al., 2004). These phenotypes are difficult to differentiate because they may occur simultaneously or sequentially in the same patient. Studies have suggested that a predominant shared component, including HLA-B27, predisposes to all phenotypic subsets, and that these subsets should be considered as various phenotypic expressions of the same disease (Said-Nahal et al., 2000, Said-Nahal et al., 2001).Braun and Sieper (2007) provided a detailed review of ankylosing spondylitis, including clinical features, pathogenesis, and management. Genetic Heterogeneity of Susceptibility to SpondyloarthropathyAdditional susceptibility loci for spondyloarthropathy have been identified on chromosome 9q31-q34 (SPDA2 ) and chromosome 2q36 (SPDA3 ).

SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1; SPDA1 Is also known as ankylosing spondylitis, susceptibility to|marie-strumpell spondylitis|bechterew syndrome

Related symptoms:

  • Pain
  • Kyphosis
  • Arrhythmia
  • Photophobia
  • Arthritis


SOURCES: OMIM ORPHANET MENDELIAN

More info about SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1; SPDA1

Medium match GENERALIZED PUSTULAR PSORIASIS


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

Medium match AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME DUE TO CTLA4 HAPLOINSUFFIENCY


Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency is a rare, primary immunodeficiency characterized by variable combination of enteropathy, hypogammaglobulinemia, recurrent respiratory infections, granulomatous lymphocytic interstitial lung disease, lymphocytic infiltration of non-lymphoid organs (intestine, lung, brain, bone marrow, kidney), autoimmune thrombocytopenia or neutropenia, autoimmune hemolytic anemia and lymphadenopathy.

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME DUE TO CTLA4 HAPLOINSUFFIENCY Is also known as alps due to ctla4 haploinsuffiency|chai|ctla4 haploinsufficiency with autoimmune infiltration|ctla-4 haploinsufficiency with autoimmune infiltration disease

Related symptoms:

  • Hepatomegaly
  • Diarrhea
  • Splenomegaly
  • Immunodeficiency
  • Recurrent infections


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME DUE TO CTLA4 HAPLOINSUFFIENCY

Medium match TAKAYASU ARTERITIS


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

Medium match EHLERS-DANLOS SYNDROME DUE TO TENASCIN-X DEFICIENCY


Ehlers-Danlos syndrome due to tenascin-X deficiency is a type of Ehlers-Danlos syndrome characterized by generalized joint hypermobility, skin hyperextensibility and easy bruising without atrophic scarring. Other common features include foot and hand deformities (piezogenic papules, pes planus, broad forefeet, brachydactyly, and acrogenic skin of hands), severe fatigue and neuromuscular symptoms including muscle weakness and myalgia.

EHLERS-DANLOS SYNDROME DUE TO TENASCIN-X DEFICIENCY Is also known as eds, classic-like type|ehlers-danlos syndrome, classic-like type|ehlers-danlos syndrome due to tenascin-x deficiency|eds due to tnx deficiency|tnx deficiency

Related symptoms:

  • Muscle weakness
  • Muscular hypotonia
  • Pain
  • Peripheral neuropathy
  • Skeletal muscle atrophy


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about EHLERS-DANLOS SYNDROME DUE TO TENASCIN-X DEFICIENCY

Medium match VELOCARDIOFACIAL 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

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

Symptoms // Phenotype % cases
Fever Uncommon - Between 30% and 50% cases
Arthralgia Uncommon - Between 30% and 50% cases
Parakeratosis Uncommon - Between 30% and 50% cases
Epidermal acanthosis Uncommon - Between 30% and 50% cases
Rheumatoid arthritis Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Skin rash Muscle weakness Inflammatory abnormality of the skin

Rare Symptoms - Less than 30% cases


Recurrent infections Thrombocytopenia Immunodeficiency Autoimmune hemolytic anemia Autoimmune thrombocytopenia Impaired T cell function Seizures Muscular hypotonia Anemia Fatigue Myalgia Aortic regurgitation Hernia Bifid uvula Vesicoureteral reflux Spina bifida Autoimmunity Inflammation of the large intestine Unilateral renal agenesis Palmoplantar pustulosis Hyperkeratosis Scaling skin Pustule Nail pits Seborrheic dermatitis Juvenile rheumatoid arthritis Pain Arrhythmia Anxiety Congenital cataract Mental deterioration Abnormality of the pinna Conductive hearing impairment Umbilical hernia Blepharophimosis Aggressive behavior Anal atresia Pulmonic stenosis Hypothyroidism Dysmetria Bulbous nose Hemolytic anemia Chorea Underdeveloped nasal alae Renal agenesis Specific learning disability Amenorrhea Peripheral demyelination Tetralogy of Fallot Psychosis Low posterior hairline Primary amenorrhea Retrognathia Photophobia Hyperactivity Hydrocephalus Hearing impairment Microcephaly Scoliosis Abnormal facial shape Cleft palate Cataract Cognitive impairment High palate Delayed speech and language development Ventricular septal defect Short neck Hypoplasia of the corpus callosum Atrial septal defect Posteriorly rotated ears Intellectual disability, severe Cerebellar atrophy Behavioral abnormality Abnormality of cardiovascular system morphology Absent speech Obesity Hypospadias Depressivity Patent ductus arteriosus Abnormal heart morphology Inguinal hernia Renal dysplasia Dementia Open mouth Multicystic kidney dysplasia Hallucinations Retinal vascular tortuosity Echolalia Abnormality of the endocrine system Pulmonary artery atresia Aplasia of the uterus Graves disease Interrupted aortic arch Perimembranous ventricular septal defect Platybasia Mood swings Right aortic arch Duodenal stenosis Paranoia Giant platelets Truncus arteriosus Velopharyngeal insufficiency Conotruncal defect Psychotic episodes Aplasia of the thymus Arteria lusoria Central nervous system degeneration Vascular ring Perineal fistula Congenital conductive hearing impairment Right aortic arch with mirror image branching Sacral meningocele Unilateral lung agenesis Myelomeningocele Pierre-Robin sequence Hypocalcemia Obsessive-compulsive behavior Short stature Narrow palpebral fissure Purpura Holoprosencephaly Bicuspid aortic valve Arnold-Chiari malformation Schizophrenia Abnormality of the hand Nasal speech Cholelithiasis Dysdiadochokinesis Apathy Acne Delusions Hypoplasia of the brainstem Myopathic facies Abnormality of the ear Basal ganglia calcification Axonal loss Submucous cleft hard palate Anal stenosis Posterior embryotoxon Bipolar affective disorder Vitiligo Hypoparathyroidism Hearing abnormality Meningocele Generalized hypotonia Ambiguous genitalia, female Global developmental delay Diffuse skin atrophy Lymphadenopathy Decreased antibody level in blood Eczema Abnormal lung morphology Lymphopenia Abnormal intestine morphology Recurrent upper respiratory tract infections Interstitial pulmonary abnormality Acute monocytic leukemia Thyroiditis Verrucae Decreased proportion of CD4-positive T cells Recurrent respiratory infections Orthokeratosis Atopic dermatitis Hypertension Dilatation Hyperhidrosis Weight loss Dermal atrophy Hypertrophic cardiomyopathy Retinopathy Neurological speech impairment Chest pain Migraine Respiratory tract infection Onychomadesis Myocardial infarction Nausea Uveitis Breathing dysregulation Chronic pain Ocular pain Hip osteoarthritis Anterior uveitis Enthesitis Sacroiliac arthritis Kyphosis Headache Erythema Nail dystrophy Nail dysplasia Splenomegaly Leukocytosis Osteomyelitis Furrowed tongue Cholangitis Chills Neutrophilia Asthenia Periostitis Geographic tongue Oligoarthritis Hepatomegaly Diarrhea Pulmonary arterial hypertension Subcutaneous nodule Intellectual disability Hiatus hernia Single transverse palmar crease Overgrowth Gastrointestinal hemorrhage Mitral valve prolapse Ambiguous genitalia Thin skin Spina bifida occulta Hyperextensible skin Atrophic scars Soft skin Adrenal hypoplasia Adrenal hyperplasia Bruising susceptibility Proximal amyotrophy Bicornuate uterus Precocious atherosclerosis Increased connective tissue Muscle fiber splitting Poor wound healing Rectal prolapse Arteriosclerosis Congenital adrenal hyperplasia Back pain Premature arteriosclerosis Quadricuspid aortic valve Sensory neuropathy Joint hypermobility Anorexia Abnormal endocardium morphology Skin ulcer Vasculitis Abnormal heart valve morphology Hemoptysis Gangrene Cerebral ischemia Reduced consciousness/confusion Abnormal aortic valve morphology Inflammatory abnormality of the eye Abnormal pattern of respiration Arterial stenosis Ascending tubular aorta aneurysm Amaurosis fugax Arachnodactyly Gastrointestinal infarctions Arteritis Hypertensive crisis Increased inflammatory response Ichthyosis Peripheral neuropathy Skeletal muscle atrophy Proximal muscle weakness Joint laxity Scarring Stroke Joint hyperflexibility Unilateral primary pulmonary dysgenesis



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