Carcinoma, and Cutaneous photosensitivity

Diseases related with Carcinoma and Cutaneous photosensitivity

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


Top matches:

High match DISSEMINATED SUPERFICIAL ACTINIC POROKERATOSIS


Disseminated superficial actinic porokeratosis (DSAP) is the most common form of porokeratosis characterized by the presence of several small annular plaques with a distinctive keratotic rim found most commonly on sun-exposed areas of the skin, particularly the extremities.

DISSEMINATED SUPERFICIAL ACTINIC POROKERATOSIS Is also known as porokeratosis, disseminated superficial actinic, 2|dsap2

Related symptoms:

  • Carcinoma
  • Pruritus
  • Cutaneous photosensitivity
  • Squamous cell carcinoma
  • Porokeratosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about DISSEMINATED SUPERFICIAL ACTINIC POROKERATOSIS

High match POROKERATOSIS OF MIBELLI


Porokeratosis of Mibelli (PM) is a form of porokeratosis that is characterized by the presence of brown single or multiple annular plaques of varying size, that are sometimes confluent, with a distinctive sharply-defined keratotic border.

POROKERATOSIS OF MIBELLI Is also known as porokeratosis of mibelli

Related symptoms:

  • Short stature
  • Neoplasm
  • Diabetes mellitus
  • Hyperkeratosis
  • Carcinoma


SOURCES: OMIM ORPHANET MENDELIAN

More info about POROKERATOSIS OF MIBELLI

High match XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC


Xeroderma pigmentosum is a genetically heterogeneous condition characterized by increased sensitivity to ultraviolet (UV) irradiation and increased risk of skin cancer resulting from a defect in DNA repair. XPC is the most common form of XP in the white population, accounting for over a third of all cases in this group (review by Li et al., 1993).For a general discussion of xeroderma pigmentosum, see XPA (OMIM ).

XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC Is also known as xp, group c|xp3|xpcc|xeroderma pigmentosum iii

Related symptoms:

  • Neoplasm
  • Hyperactivity
  • Photophobia
  • Carcinoma
  • Abnormality of the nervous system


SOURCES: OMIM MESH MENDELIAN

More info about XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC

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Other less relevant matches:

High match PORPHYRIA CUTANEA TARDA


Porphyria cutanea tarda (PCT) is characterized by light-sensitive dermatitis and the excretion of large amounts of uroporphyrin in urine (Elder et al., 1980).De Verneuil et al. (1978) and others classified porphyria cutanea tarda, the most common type of porphyria, into 2 types: type I (OMIM ), or 'sporadic' type, associated with approximately 50% level of uroporphyrinogen decarboxylase (UROD) in liver (Elder et al., 1978; Felsher et al., 1982), and type II, or 'familial' type, characterized by 50% deficient activity of the same enzyme in many tissues (Kushner et al., 1976; Elder et al., 1980).PCT type II is an autosomal dominant disorder with low penetrance and constitutes about 20% of cases of PCT. Recognized exacerbating factors of PCT include iron overload, excessive use of alcohol, exposure to polyhalogenated aromatic chemicals, exposure to estrogens, chronic viral hepatitis C, HIV infections, and mutation in the HFE gene (OMIM ) that are responsible for hereditary hemochromatosis (OMIM ) (review by Lambrecht et al., 2007).

PORPHYRIA CUTANEA TARDA Is also known as uroporphyrinogen decarboxylase deficiency|pct|pct, type ii|pct, 'familial' type|urod deficiency|porphyria cutanea tarda, type ii|porphyria, hepatocutaneous type

Related symptoms:

  • Anemia
  • Edema
  • Alopecia
  • Carcinoma
  • Erythema


SOURCES: OMIM ORPHANET MENDELIAN

More info about PORPHYRIA CUTANEA TARDA

High match ACUTE INTERMITTENT PORPHYRIA


Acute intermittent porphyria is the most frequent and the most severe form of the acute hepatic porphyrias (see this term). It is characterized by the occurrence of neuro-visceral attacks without cutaneous manifestations.

ACUTE INTERMITTENT PORPHYRIA Is also known as ups deficiency|porphyria, swedish type|pbgd deficiency|porphobilinogen deaminase deficiency|uroporphyrinogen synthase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Muscle weakness
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ACUTE INTERMITTENT PORPHYRIA

High match PORPHYRIA VARIEGATA


Variegate porphyria is a form of acute hepatic porphyria (see this term) characterized by the occurrence of neuro-visceral attacks with or without the presence of cutaneous lesions.

PORPHYRIA VARIEGATA Is also known as variegate porphyria|ppox deficiency|porphyria, south african type|protoporphyrinogen oxidase deficiency|vp

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Growth delay
  • Nystagmus


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PORPHYRIA VARIEGATA

High match BENIGN CHRONIC PEMPHIGUS; BCPM


Hailey-Hailey disease, also known as benign chronic pemphigus, is a rare autosomal dominant cutaneous disorder that usually becomes manifest in the third or fourth decade of life with erythema, vesicles, and erosions involving the body folds, particularly the groin and axillary regions. Other sites of the body, such as the neck, perianal, and submammary regions, may likewise be affected (summary by Poblete-Gutierrez et al., 2004).This disorder was first described by the dermatologist brothers Hailey and Hailey (1939).

BENIGN CHRONIC PEMPHIGUS; BCPM Is also known as hhd|hailey-hailey disease|pemphigus, benign familial

Related symptoms:

  • Intellectual disability
  • Short stature
  • Growth delay
  • Neoplasm
  • Pain


SOURCES: OMIM MENDELIAN

More info about BENIGN CHRONIC PEMPHIGUS; BCPM

High match KINDLER SYNDROME


Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes.

KINDLER SYNDROME Is also known as poikiloderma, hereditary acrokeratotic|poikiloderma of kindler|poikiloderma, congenital, with bullae, weary type|bullous acrokeratotic poikiloderma of kindler and weary|ks

Related symptoms:

  • Anemia
  • Flexion contracture
  • Dysphagia
  • Syndactyly
  • Hyperkeratosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about KINDLER SYNDROME

High match XERODERMA PIGMENTOSUM


Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV) (see these terms).

XERODERMA PIGMENTOSUM Is also known as xeroderma pigmentosum i|xp1|xp, group a|xp

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Hearing impairment
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about XERODERMA PIGMENTOSUM

Low match PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS TYPE 4


PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS TYPE 4 Is also known as pfic4|tjp2 deficit

Related symptoms:

  • Neoplasm
  • Hypertension
  • Jaundice
  • Carcinoma
  • Abnormality of the liver


SOURCES: ORPHANET OMIM MENDELIAN

More info about PROGRESSIVE FAMILIAL INTRAHEPATIC CHOLESTASIS TYPE 4

Top 5 symptoms//phenotypes associated to Carcinoma and Cutaneous photosensitivity

Symptoms // Phenotype % cases
Squamous cell carcinoma Common - Between 50% and 80% cases
Neoplasm Common - Between 50% and 80% cases
Hypopigmentation of the skin Uncommon - Between 30% and 50% cases
Hepatocellular carcinoma Uncommon - Between 30% and 50% cases
Abnormal blistering of the skin Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Carcinoma and Cutaneous photosensitivity. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Erythema Anemia Poikiloderma Telangiectasia Intellectual disability Short stature Hyperkeratosis Alopecia Hypopigmented skin patches Diarrhea Thin skin Vomiting Neoplasm of the skin Hypertension Pain Ectropion Dermal atrophy Melanoma Conjunctivitis Fragile skin Seizures Pruritus

Rare Symptoms - Less than 30% cases


Muscle weakness Arthralgia Depressivity Dry skin Constipation Hyperhidrosis Abdominal pain Abnormality of the dentition Paralysis Growth delay Milia Hypogonadism Abnormality of skin pigmentation Scarring Fever Peripheral neuropathy Porphyrinuria Nausea and vomiting Agitation Hallucinations Psychosis Tachycardia Cataract Eczema Nausea Insomnia Anxiety Freckling Inflammatory abnormality of the skin Basal cell carcinoma Keratitis Entropion Photophobia Defective DNA repair after ultraviolet radiation damage Edema Abnormality of the liver Cirrhosis Aplasia/Hypoplasia of the skin Hepatitis Hypertrichosis Skin rash Porokeratosis Atypical scarring of skin Skin vesicle Abnormality of the hand Ridged nail Short 5th metacarpal Ankyloglossia Premature loss of primary teeth Ichthyosis Cholestasis Cheilitis Overbite Esophageal stricture Palmoplantar keratoderma Eczematoid dermatitis Hepatic failure Abnormality of the anus Laryngeal stenosis Urethral stricture Carious teeth Nail dystrophy Spotty hypopigmentation Amniotic constriction ring Short 4th metacarpal Portal hypertension Abnormality of the skull Atrophic scars Colitis Recurrent skin infections Intermittent jaundice Palmoplantar hyperkeratosis Cutaneous finger syndactyly Gingival bleeding Turricephaly Gingivitis Inflammation of the large intestine Intrahepatic cholestasis Abnormality of dental enamel Periodontitis Phimosis Esophagitis Acute hepatic failure Abnormality of the ribs Abnormal toenail morphology Corneal erosion Hypermelanotic macule Acral blistering Spotty hyperpigmentation Abnormal vertebral morphology Finger syndactyly Developmental regression Decreased testicular size Neoplasm of the eye Abnormality of extrapyramidal motor function Ankyloblepharon Papilloma Choreoathetosis Thickened skin Bone marrow hypocellularity EEG abnormality Conjunctival telangiectasia Craniofacial hyperostosis Blepharitis Aminoaciduria Telangiectasia of the skin Opacification of the corneal stroma Macule Intellectual disability, progressive Reduced tendon reflexes Pterygium Mental deterioration Cerebral cortical atrophy Severe photosensitivity Ataxia Symblepharon Overjet Diffuse skin atrophy Melanocytic nevus Telangiectases in sun-exposed and nonexposed skin Neoplasm of the urethra Hearing impairment Microcephaly Scoliosis Jaundice Delayed skeletal maturation Failure to thrive Strabismus Sensorineural hearing impairment Cryptorchidism Spasticity Flat nasal alae Cognitive impairment Optic atrophy Fatigue Hyporeflexia Papule Restlessness Corneal opacity Nephropathy Intellectual disability, mild Renal insufficiency Arrhythmia Weight loss Hepatosplenomegaly Myalgia Lethargy Paresthesia Stage 5 chronic kidney disease Coma Global developmental delay Abdominal distention Urinary incontinence Anorexia Paraparesis Hyperlipidemia Cranial nerve paralysis Hyponatremia Apathy Dysuria Behavioral abnormality Hyperpigmentation in sun-exposed areas Urinary retention Hepatic steatosis Diabetes mellitus Prematurely aged appearance Abnormality of chromosome stability Hyperactivity Abnormality of the nervous system Systemic lupus erythematosus Squamous cell carcinoma of the skin Cutaneous melanoma Hemolytic anemia Sudden cardiac death Viral hepatitis Hyperpigmentation of the skin Generalized hirsutism Cerebral palsy Scleroderma Onycholysis Anemia of inadequate production Alcoholism Congenital hypoplastic anemia Facial hypertrichosis Ileus Diaphragmatic paralysis Camptodactyly of finger Striae distensae Prominent forehead Osteoporosis Osteopenia Postnatal growth retardation Sparse hair Leukemia Overgrowth Sparse scalp hair Erythroderma Severe vision loss Visual impairment Alopecia of scalp Osteosarcoma Concave nasal ridge Acantholysis Lamellar cataract Acrokeratosis Flexion contracture Dysphagia Syndactyly Frontal bossing Feeding difficulties Abnormal urinary color Abnormality of the skeletal system Delirium Psychotic episodes Hypertensive crisis Respiratory paralysis Paralytic ileus Elevated urinary delta-aminolevulinic acid Red urine Acute episodes of neuropathic symptoms Nystagmus Clinodactyly Premature adrenarche Abnormality of the kidney Confusion Tetraplegia Aspiration Chronic kidney disease Visual hallucinations Neoplasm of the liver Motor polyneuropathy Dark urine Biliary atresia



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