Arthritis, and Palmoplantar keratoderma

Diseases related with Arthritis and Palmoplantar keratoderma

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


Top matches:

Low match BUSCHKE-OLLENDORFF SYNDROME


Buschke-Ollendorff syndrome (BOS) is a benign disorder characterized by the association of osteopoikilosis lesions (``spotted bones'') in the skeleton and connective tissue nevi in the skin.

BUSCHKE-OLLENDORFF SYNDROME Is also known as dermatofibrosis, disseminated, with osteopoikilosis|osteopathia condensans disseminata|dermatoosteopoikilosis|dermatofibrosis lenticularis disseminata with osteopoikilosis|disseminated dermatofibrosis with osteopoikilosis

Related symptoms:

  • Short stature
  • Hearing impairment
  • Strabismus
  • Pain
  • Flexion contracture


SOURCES: ORPHANET OMIM MENDELIAN

More info about BUSCHKE-OLLENDORFF SYNDROME

Low match PACHYDERMOPERIOSTOSIS


Pachydermoperiostosis (PDP) is a form of primary hypertrophic osteoarthropathy (see this term), a rare hereditary disorder, and is characterized by digital clubbing, pachydermia and subperiosteal new bone formation associated with pain, polyarthritis, cutis verticis gyrata, seborrhea and hyperhidrosis. Three forms have been described: a complete form with pachydermia and periostitis, an incomplete form with evidence of bone abnormalities but lacking pachydermia, and a forme frusta with prominent pachydermia and minimal-to-absent skeletal changes.

PACHYDERMOPERIOSTOSIS Is also known as touraine-solente-gole syndrome|pdp

Related symptoms:

  • Scoliosis
  • Ptosis
  • Anemia
  • Hepatomegaly
  • Edema


SOURCES: ORPHANET MENDELIAN

More info about PACHYDERMOPERIOSTOSIS

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

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Other less relevant matches:

Low match KERATOSIS PALMOPLANTARIS STRIATA III; PPKS3


KERATOSIS PALMOPLANTARIS STRIATA III; PPKS3 Is also known as kpps3|keratoderma, palmoplantar, striate form iii|striate palmoplantar keratoderma iii|sppk3

Related symptoms:

  • Palmoplantar keratoderma


SOURCES: OMIM MESH MENDELIAN

More info about KERATOSIS PALMOPLANTARIS STRIATA III; PPKS3

Low match STRIATE PALMOPLANTAR KERATODERMA


Striate palmoplantar keratoderma is an isolated, focal, hereditary palmoplantar keratoderma characterized by linear hyperkeratosis along the flexor aspect of the fingers and on palms, as well as focal hyperkeratosis of the plantar skin. Patients present with painful thickening of the skin on palms and soles, with occasional fissuring, blistering and hyperhidrosis. Rarely, hyperkeratosis on other areas may be seen (knees, dorsal aspects of the digits). Histopatologically, widened intercellular spaces between keratinocytes are observed.

STRIATE PALMOPLANTAR KERATODERMA Is also known as keratosis palmoplantaris striata et areata|keratosis palmoplantaris varians of wachters|keratosis palmoplantaris striata

Related symptoms:

  • Palmoplantar keratoderma
  • Abnormality of the hair
  • Abnormality of the nail


SOURCES: ORPHANET MENDELIAN

More info about STRIATE PALMOPLANTAR KERATODERMA

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 PSORIASIS 2; PSORS2


Related symptoms:

  • Fever
  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Ichthyosis


SOURCES: OMIM MENDELIAN

More info about PSORIASIS 2; PSORS2

Low match PROGRESSIVE SYMMETRIC ERYTHROKERATODERMIA


PROGRESSIVE SYMMETRIC ERYTHROKERATODERMIA Is also known as darier-gottron disease|progressive symmetric erythrokeratodermia, gottron type|erythrokeratodermia progressiva symmetrica

Related symptoms:

  • Erythema
  • Palmoplantar keratoderma
  • Skin plaque


SOURCES: ORPHANET MENDELIAN

More info about PROGRESSIVE SYMMETRIC ERYTHROKERATODERMIA

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

Top 5 symptoms//phenotypes associated to Arthritis and Palmoplantar keratoderma

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

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

Rare Symptoms - Less than 30% cases


Diffuse skin atrophy Hyperhidrosis Thickened skin Osteolysis Neoplasm of the skin Seborrheic dermatitis Short stature Hearing impairment Bone pain Scarring Scaling skin Epidermal acanthosis Psoriasiform dermatitis Parakeratosis Atopic dermatitis Abnormal cortical bone morphology Alopecia Abnormality of the dentition Abnormality of epiphysis morphology Skeletal muscle atrophy Visual impairment Pain Papule Abnormal eyebrow morphology Hypoplastic toenails Oral leukoplakia Hypoplastic fingernail Furrowed tongue Dystrophic toenail Corneal erosion Abnormal eyelash morphology Alopecia of scalp Keratoconjunctivitis sicca Severe hearing impairment Cellulitis Macule Aplasia/Hypoplasia of the eyebrow Squamous cell carcinoma Hemiplegia/hemiparesis Absent eyebrow Corneal neovascularization Keratitis Congenital sensorineural hearing impairment Sunken cheeks Urticaria Reduced tendon reflexes Sparse eyelashes Conjunctivitis Knee flexion contracture Elbow flexion contracture Skin ulcer Sparse and thin eyebrow Hypohidrosis Aganglionic megacolon Fine hair Dystrophic fingernails Recurrent corneal erosions Absent eyelashes Flexion contracture Aplasia/Hypoplasia of the skin Epiphora Follicular hyperkeratosis Spinal muscular atrophy Sparse eyebrow Hypotrichosis Pectus excavatum Skin plaque Orthokeratosis Strabismus Rheumatoid arthritis Dermal atrophy Fever Folliculitis Comedo Abnormality of the tongue Corneal ulceration Squamous cell carcinoma of the skin Nail dysplasia Keratoconjunctivitis Corneal scarring Recurrent bacterial skin infections Generalized hyperkeratosis Moderate hearing impairment Hypertension Trichiasis Abnormality of corneal stroma Abnormality of the hair Abnormality of the nail Skin rash Overgrowth Progressive visual loss Lymphedema Delayed eruption of teeth Coarse facial features Anemia Hepatomegaly Edema Splenomegaly Osteoporosis Abnormality of the metaphysis Malabsorption Scoliosis Small hand Limitation of joint mobility Gastrointestinal hemorrhage Nevus Gynecomastia Abnormality of the fingernails Ptosis Abnormal axial skeleton morphology Cerebral palsy Atypical scarring of skin Hemangioma Flat occiput Hyperostosis Multiple lipomas Scleroderma Cutaneous finger syndactyly Generalized hypopigmentation Complete duplication of the distal phalanges of the hand Generalized osteosclerosis Abnormal aortic morphology Generalized limb muscle atrophy Abnormal bone structure Osteopoikilosis Connective tissue nevi Subcutaneous nodule Recurrent fractures Genu varum Hoarse voice Photophobia Visual loss Delayed skeletal maturation Joint stiffness Cerebellar hypoplasia Pes cavus Myalgia Carcinoma Cryptorchidism Skeletal dysplasia Sparse hair Renal insufficiency Severe global developmental delay Nail dystrophy Carious teeth Blindness Sensorineural hearing impairment Acne Craniosynostosis Osteomyelitis Aseptic necrosis Joint swelling Growth hormone excess Neoplasm of the lung Abnormal hair pattern Peptic ulcer Neoplasm Abnormal hair quantity Eczematoid dermatitis Abnormality of bone marrow cell morphology Cutis gyrata of scalp Clubbing of toes Impaired temperature sensation Intellectual disability Abnormal perifollicular morphology



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