Arthritis, and Ichthyosis

Diseases related with Arthritis and Ichthyosis

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


Top matches:

Low match PSORIASIS 2; PSORS2


Related symptoms:

  • Fever
  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Ichthyosis


SOURCES: OMIM MENDELIAN

More info about PSORIASIS 2; PSORS2

Low match ULERYTHEMA OPHRYOGENESIS


Ulerythema ophryogenesis is characterised by inflammatory keratotic papules occurring on the face, which may be followed by scars, atrophy and alopecia. Prevalence is unknown but the disease, affecting mainly children and young adults, is rare. Erythema with mild hyperkeratosis of the hair follicles resulting in rough papules is observed on the cheeks and lateral aspects of the eyebrows. The disorder occasionally extends to the adjacent scalp, ears and forehead and rarely to the extensor surfaces of the limbs. Symptoms regress with age, although loss of the lateral aspects of the eyebrows can occur. Many cases occur sporadically; autosomal dominant inheritance has also been reported. There is no particular treatment, but patients should avoid sun exposure without UV protection.

Related symptoms:

  • Skeletal muscle atrophy
  • Pectus excavatum
  • Alopecia
  • Arthritis
  • Erythema


SOURCES: ORPHANET OMIM MENDELIAN

More info about ULERYTHEMA OPHRYOGENESIS

Low match HARLEQUIN ICHTHYOSIS


Harlequin ichthyosis (HI) is the most severe variant of autosomal recessive congenital ichthyosis (ARCI; see this term). It is characterized at birth by the presence of large, thick, plate-like scales over the whole body associated with severe ectropion, eclabium, and flattened ears, that later develops into a severe scaling erythroderma.

HARLEQUIN ICHTHYOSIS Is also known as ichthyosis congenita, harlequin type|'harlequin fetus'|ichthyosis congenita, harlequin fetus type|harlequin ichthyosis|ichthyosis fetalis, harlequin type|hi

Related symptoms:

  • Global developmental delay
  • Cataract
  • Respiratory insufficiency
  • Recurrent respiratory infections
  • Respiratory failure


SOURCES: OMIM ORPHANET MENDELIAN

More info about HARLEQUIN ICHTHYOSIS

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Other less relevant matches:

Low match MUCKLE-WELLS SYNDROME; MWS


Muckle-Wells syndrome (MWS) is characterized by episodic skin rash, arthralgias, and fever associated with late-onset sensorineural deafness and renal amyloidosis (Dode et al., 2002).See also familial cold-induced autoinflammatory syndrome-1 (FCAS1, CAPS1; {120100}), an allelic disorder with overlapping clinical features.

MUCKLE-WELLS SYNDROME; MWS Is also known as caps2|uda syndrome|urticaria-deafness-amyloidosis syndrome|cryopyrin-associated periodic syndrome 2

Related symptoms:

  • Seizures
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain
  • Anemia


SOURCES: OMIM MENDELIAN

More info about MUCKLE-WELLS SYNDROME; MWS

Low match MUCKLE-WELLS SYNDROME


Muckle-Wells syndrome (MWS) is an intermediate form of cryopyrin-associated periodic syndrome (CAPS; see this term) and is characterized by recurrent fever (with malaise and chills), recurrent urticaria-like skin rash, sensorineural deafness, general signs of inflammation (eye redness, headaches, arthralgia/myalgia) and potentially life-threatening secondary amyloidosis (AA type).

MUCKLE-WELLS SYNDROME Is also known as neutrophilic urticaria

Related symptoms:

  • Short stature
  • Anemia
  • Hepatomegaly
  • Fever
  • Optic atrophy


SOURCES: ORPHANET MENDELIAN

More info about MUCKLE-WELLS SYNDROME

Low match KID SYNDROME


Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.

KID SYNDROME Is also known as ichthyosis hystrix rheydt type|keratitis-ichthyosis-deafness/hystrix-like ichthyosis-deafness syndrome|senter syndrome|kid/hid syndrome|kid syndrome, autosomal dominant

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Neoplasm
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about KID SYNDROME

Low match BATHING SUIT ICHTHYOSIS


Bathing suit ichthyosis (BSI) is a rare variant of autosomal recessive congenital ichthyosis (ARCI; see this term) characterized by the presence of large dark scales in specific areas of the body.

BATHING SUIT ICHTHYOSIS Is also known as bsi

Related symptoms:

  • Ichthyosis


SOURCES: ORPHANET MENDELIAN

More info about BATHING SUIT ICHTHYOSIS

Low match ACRAL SELF-HEALING COLLODION BABY


Acral self-healing collodion baby (SHCB) is a variant of SHCB (see this term) characterized by the presence at birth of a collodion membrane only at the extremities.

ACRAL SELF-HEALING COLLODION BABY Is also known as acral shcb

Related symptoms:

  • Ichthyosis


SOURCES: ORPHANET MENDELIAN

More info about ACRAL SELF-HEALING COLLODION BABY

Low 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

Low match COMPLEMENT COMPONENT 7 DEFICIENCY; C7D


COMPLEMENT COMPONENT 7 DEFICIENCY; C7D Is also known as c7 deficiency

Related symptoms:

  • Fever
  • Arthritis
  • Telangiectasia
  • Meningitis
  • Vasculitis


SOURCES: OMIM MESH MENDELIAN

More info about COMPLEMENT COMPONENT 7 DEFICIENCY; C7D

Top 5 symptoms//phenotypes associated to Arthritis and Ichthyosis

Symptoms // Phenotype % cases
Fever Uncommon - Between 30% and 50% cases
Arthralgia Uncommon - Between 30% and 50% cases
Hyperkeratosis Uncommon - Between 30% and 50% cases
Vasculitis Uncommon - Between 30% and 50% cases
Inflammatory abnormality of the skin Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Skin rash Urticaria Conjunctivitis

Rare Symptoms - Less than 30% cases


Hearing impairment Progressive sensorineural hearing impairment Elevated erythrocyte sedimentation rate Thickened skin Meningitis Nephrotic syndrome Nephropathy Short stature Myalgia Abdominal pain Anemia Pain Renal amyloidosis Recurrent aphthous stomatitis Sensorineural hearing impairment Scaling skin Parakeratosis Pes cavus Alopecia Erythema Scarring Psoriasiform dermatitis Atopic dermatitis Epidermal acanthosis Aganglionic megacolon Fine hair Palmoplantar keratoderma Abnormality of the nose Progressive visual loss Hypohidrosis Sparse and thin eyebrow Nail dysplasia Skin ulcer Broad foot Delayed eruption of teeth Abnormality of the dentition Carious teeth Hyperhidrosis Visual loss Visual impairment Cryptorchidism Delayed skeletal maturation Cerebellar hypoplasia Neoplasm Photophobia Episcleritis Carcinoma Sparse hair Severe global developmental delay Nail dystrophy Intellectual disability Blindness Hernia of the abdominal wall Congenital sensorineural hearing impairment Elbow flexion contracture Overgrowth Squamous cell carcinoma of the skin Keratoconjunctivitis Corneal scarring Recurrent bacterial skin infections Generalized hyperkeratosis Corneal ulceration Moderate hearing impairment Trichiasis Abnormality of corneal stroma Seborrheic dermatitis Recurrent corneal erosions Telangiectasia Raynaud phenomenon Complement deficiency Pyoderma Sclerodactyly Vasculitis in the skin Subcutaneous calcification Recurrent meningococcal disease Recurrent meningitis C8 deficiency Abnormality of the tongue Corneal neovascularization Knee flexion contracture Aplasia/Hypoplasia of the eyebrow Sparse eyelashes Osteolysis Neoplasm of the skin Reduced tendon reflexes Restrictive ventilatory defect Keratitis Absent eyebrow Hypoplastic toenails Hemiplegia/hemiparesis Squamous cell carcinoma Macule Dystrophic fingernails Cellulitis Severe hearing impairment Keratoconjunctivitis sicca Alopecia of scalp Abnormal eyelash morphology Corneal erosion Dystrophic toenail Furrowed tongue Hypoplastic fingernail Oral leukoplakia Uveitis Band keratopathy Abnormality of the voice Sepsis Respiratory insufficiency Recurrent respiratory infections Respiratory failure Proptosis Rigidity Small for gestational age Everted lower lip vermilion Sudden cardiac death Global developmental delay Limitation of joint mobility Premature birth Dehydration Depressed nasal ridge Recurrent skin infections Hand polydactyly Ectropion Cataract Abnormal perifollicular morphology Erythroderma Hypotrichosis Dermal atrophy Rheumatoid arthritis Orthokeratosis Diffuse skin atrophy Skeletal muscle atrophy Pectus excavatum Papule Sparse eyebrow Sunken cheeks Spinal muscular atrophy Epiphora Aplasia/Hypoplasia of the skin Absent eyelashes Abnormal eyebrow morphology Follicular hyperkeratosis Folliculitis Comedo Self-injurious behavior Short finger Abnormal palate morphology Optic atrophy Abnormality of the mouth Papilledema Microscopic hematuria Chills Cystinuria Rigors Hepatomegaly Macrocephaly Amyloidosis Splenomegaly Abnormality of metabolism/homeostasis Glaucoma Camptodactyly of finger Delayed puberty Abnormality of the genital system Cranial nerve paralysis Episodic fever Leukocytosis Congenital ichthyosiform erythroderma Seizures Foot polydactyly Malignant hyperthermia Hearing abnormality Lack of skin elasticity Congenital nonbullous ichthyosiform erythroderma Hypergranulosis Eclabion Fatigue Abnormality of the skin Abnormality of the skeletal system Diarrhea Renal insufficiency Hepatosplenomegaly Lymphadenopathy Stage 5 chronic kidney disease Hematuria Coma Pyoderma gangrenosum



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