Fever, and Eczema

Diseases related with Fever and Eczema

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

Top matches:

Bronchial asthma is the most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment.Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002; Pillai et al., 2006). See {147050} for information on the asthma-associated phenotype atopy.

ASTHMA, SUSCEPTIBILITY TO Is also known as asthma, bronchial|asthma-related traits, susceptibility to

Related symptoms:

  • Fever
  • Respiratory distress
  • Dyspnea
  • Cough
  • Asthma


SOURCES: OMIM MENDELIAN

More info about ASTHMA, SUSCEPTIBILITY TO

Medium match ICHTHYOSIS VULGARIS

The most common form of ichthyosis. It is an autosomal dominant inherited or acquired disorder characterized by scaling and desquamation of the skin.

ICHTHYOSIS VULGARIS Is also known as ichthyosis simplex

Related symptoms:

  • Fever
  • Hyperkeratosis
  • Ichthyosis
  • Asthma
  • Eczema


SOURCES: OMIM MESH MENDELIAN

More info about ICHTHYOSIS VULGARIS

X-linked severe congenital neutropenia is an immunodeficiency syndrome characterized by recurrent major bacterial infections, severe congenital neutropenia, and monocytopenia. It has been described in five males spanning three generations of one family. It is transmitted as an X-linked recessive trait and is caused by mutations in the WAS gene, encoding the WASP protein.

X-LINKED SEVERE CONGENITAL NEUTROPENIA Is also known as xln

Related symptoms:

  • Fever
  • Immunodeficiency
  • Neutropenia
  • Abnormality of the skin
  • Eczema


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about X-LINKED SEVERE CONGENITAL NEUTROPENIA

Other less relevant matches:

Autosomal recessive cytochrome b-positive chronic granulomatous disease (CGD) type III is a immunodeficiency disorder characterized by recurrent pyogenic infections and granulomatous inflammation resulting from loss of phagocyte superoxide production (summary by Matute et al., 2009).For a general phenotypic description and a discussion of genetic heterogeneity of chronic granulomatous disease, see the well-established X-linked recessive cytochrome b-negative form (CGD ).

X-LINKED MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASES DUE TO CYBB DEFICIENCY Is also known as granulomatous disease, chronic, due to ncf4 deficiency|cgd, autosomal recessive cytochrome b-positive, type iii|x-linked msmd due to cybb deficiency

Related symptoms:

  • Fever
  • Diarrhea
  • Immunodeficiency
  • Skin rash
  • Eczema


SOURCES: OMIM ORPHANET MENDELIAN

More info about X-LINKED MENDELIAN SUSCEPTIBILITY TO MYCOBACTERIAL DISEASES DUE TO CYBB DEFICIENCY

T-B+ SEVERE COMBINED IMMUNODEFICIENCY DUE TO IL-7RALPHA DEFICIENCY Is also known as scid, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive|t-b+ scid due to il-7ralpha deficiency

Related symptoms:

  • Growth delay
  • Failure to thrive
  • Hepatomegaly
  • Fever
  • Diarrhea


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about T-B+ SEVERE COMBINED IMMUNODEFICIENCY DUE TO IL-7RALPHA DEFICIENCY

Chronic granulomatous disease (CGD) is a rare primary immunodeficiency, mainly affecting phagocytes, which is characterized by an increased susceptibility to severe and recurrent bacterial and fungal infections, along with the development of granulomas.

CHRONIC GRANULOMATOUS DISEASE Is also known as chronic septic granulomatosis|cgd

Related symptoms:

  • Hepatomegaly
  • Fever
  • Splenomegaly
  • Recurrent respiratory infections
  • Malabsorption


SOURCES: ORPHANET MENDELIAN

More info about CHRONIC GRANULOMATOUS DISEASE

Combined immunodeficiency (CID) due to STIM1 deficiency is a form of CID due to Calcium release activated Ca2+(CRAC) channel dysfunction (see this term) characterized by recurrent infections, autoimmunity, congenital myopathy and ectodermal dysplasia.

COMBINED IMMUNODEFICIENCY DUE TO STIM1 DEFICIENCY Is also known as cid due to stim1 deficiency|immune dysfunction with t-cell inactivation due to calcium entry defect 2|stim1 deficiency

Related symptoms:

  • Generalized hypotonia
  • Muscular hypotonia
  • Anemia
  • Myopathy
  • Diarrhea


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about COMBINED IMMUNODEFICIENCY DUE TO STIM1 DEFICIENCY

Pyogenic bacterial infection due to MyD88 deficiency is a primary immunodeficiency characterized by increased susceptibility to pyogenic bacterial infections, including invasive pneumococcal, invasive staphylococcal and pseudomonas disease.

PYOGENIC BACTERIAL INFECTIONS DUE TO MYD88 DEFICIENCY Is also known as myd88 deficiency|pyogenic bacterial infections, recurrent, due to myd88 deficiency|recurrent pyogenic bacterial infections due to myd88 deficiency

Related symptoms:

  • Fever
  • Immunodeficiency
  • Recurrent bacterial skin infections


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about PYOGENIC BACTERIAL INFECTIONS DUE TO MYD88 DEFICIENCY

Medium match BLAU SYNDROME; BLAUS

Blau syndrome is characterized by the triad of granulomatous arthritis, uveitis, and dermatitis. First described in 1985, it was considered to be distinct from sarcoidosis due to the early age of onset and autosomal dominant inheritance pattern. Published reports of sporadic cases of children with 'early-onset sarcoidosis' (EOS) with granulomatous involvement of different organs, primarily affecting joints, eyes, and skin, were suspected to represent the same disorder because the patients' characteristics were nearly identical. Subsequently, identical NOD2 mutations were identified in patients with Blau syndrome as well as in patients diagnosed with EOS, confirming earlier suspicions that they represented the same disease (summary by Borzutzky et al., 2010). Unlike older children diagnosed with sarcoidosis, these patients have no apparent pulmonary involvement; however, the disease is progressive and may result in severe complications such as blindness and/or joint destruction (Shetty and Gedalia, 1998).

BLAU SYNDROME; BLAUS Is also known as arthrocutaneouveal granulomatosis|granulomatous inflammatory arthritis, dermatitis, and uveitis, familial|eos|jabs syndrome|granulomatosis, familial juvenile systemic|acug|sarcoidosis, early-onset|granulomatosis, familial, blau type

Related symptoms:

  • Hearing impairment
  • Failure to thrive
  • Cataract
  • Flexion contracture
  • Visual impairment


SOURCES: OMIM MENDELIAN

More info about BLAU SYNDROME; BLAUS

Chronic mucocutaneous candidosis (CMC) refers to a group of heterogenous disorders characterized by persistent, debilitating and/or recurrent infections of the skin, nails, and mucus membranes, mainly with the fungal pathogen Candida albicans.

CHRONIC MUCOCUTANEOUS CANDIDIASIS Is also known as card9 immunodeficiency|candidiasis, familial chronic mucocutaneous, autosomal recessive|cmc

Related symptoms:

  • Seizures
  • Fever
  • Behavioral abnormality
  • Immunodeficiency
  • Headache


SOURCES: OMIM ORPHANET MENDELIAN

More info about CHRONIC MUCOCUTANEOUS CANDIDIASIS

Top 5 symptoms//phenotypes associated to Fever and Eczema

Symptoms // Phenotype % cases
Immunodeficiency Uncommon - Between 30% and 50% cases
Inflammatory abnormality of the skin Uncommon - Between 30% and 50% cases
Skin rash Uncommon - Between 30% and 50% cases
Asthma Uncommon - Between 30% and 50% cases
Recurrent bacterial infections Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Lymphadenopathy Cough Diarrhea Skin ulcer

Rare Symptoms - Less than 30% cases

Hyperkeratosis Allergic rhinitis Recurrent respiratory infections Otitis media Hepatosplenomegaly Splenomegaly Hepatomegaly Failure to thrive Sinusitis Meningitis Recurrent infections Autoimmunity Abnormality of the skin Epidermal acanthosis Abnormality of dental enamel Papule Glaucoma Camptodactyly Iritis Iridocyclitis Posterior uveitis Rheumatoid arthritis Anterior uveitis Band keratopathy Granulomatosis Flexion contracture of toe Abducens palsy Cystoid macular edema Synovitis Juvenile rheumatoid arthritis Edema Abnormality of the ear Camptodactyly of finger Macular edema Hypercalcemia Subcutaneous nodule Peripheral neuropathy Abnormal cranial nerve morphology Joint swelling Arthritis Uveitis Optic neuropathy Blindness Abnormal joint morphology Increased antibody level in blood Vasculitis Abnormality of the eye Large vessel vasculitis Cheilitis Hemoptysis Abnormality of the mouth Abnormal toenail morphology Chronic mucocutaneous candidiasis Abnormal vagina morphology Lichenification Recurrent fungal infections Abnormality of the immune system Abnormal endocardium morphology Abnormality of temperature regulation Onychomycosis Abnormal lip morphology Dyspareunia Broad nail Abnormality of blood and blood-forming tissues Abnormality of vision Panuveitis Visual impairment Tendonitis Intermittent generalized erythematous papular rash Nongranulomatous uveitis Seizures Behavioral abnormality Headache Feeding difficulties in infancy Abnormality of the fingernails Erythema Pruritus Hematuria Hepatitis Recurrent urinary tract infections Abnormality of the nail Hypertension Recurrent pneumonia Flexion contracture Recurrent sinusitis Failure to thrive secondary to recurrent infections Recurrent opportunistic infections Oral ulcer Decrease in T cell count Severe combined immunodeficiency Increased body weight Recurrent otitis media Pancytopenia Gastroesophageal reflux Growth delay Perianal rash Perioral eczema Low-grade fever Recurrent aphthous stomatitis Colitis Sepsis Heat intolerance Dyspnea Wheezing Atopic dermatitis Chest tightness Ichthyosis Scaling skin Eczematoid dermatitis Monocytopenia Orthokeratotic hyperkeratosis Neutropenia Myelodysplasia Anisocytosis Increased mean platelet volume Congenital neutropenia Malabsorption Cutaneous photosensitivity Cataract Nail dysplasia Hearing impairment Recurrent bacterial skin infections Intermittent diarrhea Recurrent lower respiratory tract infections Amelogenesis imperfecta Hypoplasia of the iris Episodic fever Autoimmune hemolytic anemia Anhidrosis Sarcoma Respiratory distress Hypohidrosis Hypoplasia of dental enamel Nephrotic syndrome Hemolytic anemia Pyloric stenosis Mediastinal lymphadenopathy Tracheoesophageal fistula Hypermelanotic macule Macule Gingivitis Chronic obstructive pulmonary disease Inflammatory abnormality of the eye Abnormality of neutrophils Pneumonia Liver abscess Generalized hypotonia Muscular hypotonia Anemia Myopathy Thrombocytopenia Chronic oral candidiasis


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