Carcinoma, and Carious teeth

Diseases related with Carcinoma and Carious teeth

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


Top matches:

High match FAMILIAL CUTANEOUS TELANGIECTASIA AND OROPHARYNGEAL CANCER PREDISPOSITION SYNDROME


Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome is a rare, inherited cancer-predisposing syndrome characterized by an early development of cutaneous telangiectasia, mild dental and nail anomalies, patchy alopecia over the affected skin areas and increased lifetime risk for oropharyngeal cancer. Other types of cancer have also been reported.

FAMILIAL CUTANEOUS TELANGIECTASIA AND OROPHARYNGEAL CANCER PREDISPOSITION SYNDROME Is also known as telangiectasia, cutaneous, and cancer syndrome, familial

Related symptoms:

  • Neoplasm
  • Alopecia
  • Carcinoma
  • Carious teeth
  • Convex nasal ridge


SOURCES: ORPHANET OMIM MENDELIAN

More info about FAMILIAL CUTANEOUS TELANGIECTASIA AND OROPHARYNGEAL CANCER PREDISPOSITION SYNDROME

High match DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1


Dyskeratosis congenita is a bone marrow failure syndrome classically characterized by the triad of abnormal skin pigmentation, nail dystrophy, and leukoplakia of the oral mucosa. Progressive bone marrow failure occurs in over 80% of cases and is the main cause of early mortality. The phenotype is highly variable, and affected individuals may have multiple additional features, including pulmonary fibrosis, liver cirrhosis, premature hair loss and/or graying, osteoporosis, atresia of the lacrimal ducts, and learning difficulties. Predisposition to malignancy is an important feature. The disorder is caused by defects in the maintenance of telomeres (summary by Kirwan and Dokal, 2008).For a discussion of genetic heterogeneity of dyskeratosis congenita, see DKCA1 (OMIM ).

Related symptoms:

  • Intellectual disability
  • Microcephaly
  • Abnormality of the dentition
  • Thrombocytopenia
  • Alopecia


SOURCES: MESH OMIM MENDELIAN

More info about DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1; DKCB1

High match WHIM SYNDROME


WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome is a congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

WHIM SYNDROME Is also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome|warts-infections-leukopenia-myelokatexis syndrome|wilm|warts-hypogammaglobulinemia-infections-myelokathexis syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Fever
  • Congestive heart failure
  • Immunodeficiency


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WHIM SYNDROME

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Other less relevant matches:

High match CRISPONI/COLD-INDUCED SWEATING SYNDROME 2; CISS2


Crisponi/cold-induced sweating syndrome is an autosomal recessive disorder characterized in the neonatal period by orofacial weakness with impaired sucking and swallowing resulting in poor feeding necessitating medical intervention. Affected infants show a tendency to startle, with contractions of the facial muscles in response to tactile stimuli or during crying, trismus, abundant salivation, and opisthotonus. During the first year, most infants have spiking fevers. These features, referred to as 'Crisponi syndrome' in infancy, can result in early death without advanced care. After the first 2 years, the abnormal muscle contractions and fevers abate, and most patients show normal psychomotor development. From childhood onward, the most disabling symptoms stem from impaired thermoregulation and disabling abnormal sweating, which can be treated with clonidine. Patients have hyperhidrosis, mainly of the upper body, in response to cold temperatures, and sweat very little with heat. Other features include characteristic facial anomalies, such as round face, chubby cheeks, micrognathia, high-arched palate, low-set ears, and depressed nasal bridge, dental decay, camptodactyly, and progressive kyphoscoliosis (summary by Hahn et al., 2010).For a discussion of genetic heterogeneity of Crisponi/cold-induced sweating syndrome, see CISS1 (OMIM ).

Related symptoms:

  • Scoliosis
  • Micrognathia
  • Muscle weakness
  • Pain
  • Low-set ears


SOURCES: OMIM MESH MENDELIAN

More info about CRISPONI/COLD-INDUCED SWEATING SYNDROME 2; CISS2

High match PAPILLON-LEFÈVRE SYNDROME


Papillon-Lefèvre syndrome (PLS) is a rare ectodermal dysplasia characterized by palmoplantar keratoderma associated with early-onset periodontitis.

PAPILLON-LEFÈVRE SYNDROME Is also known as keratosis palmoplantar-periodontopathy syndrome|pls|keratosis palmoplantaris with periodontopathia

Related symptoms:

  • Intellectual disability
  • Neoplasm
  • Abnormality of the dentition
  • Recurrent respiratory infections
  • Hyperhidrosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PAPILLON-LEFÈVRE SYNDROME

High match SEVERE GENERALIZED RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA


Severe generalized recessive dystrophic epidermolysis bullosa (RDEB-sev gen) is the most severe subtype of dystrophic epidermolysis bullosa (DEB, see this term), formerly known as the Hallopeau-Siemens type, and is characterized by generalized cutaneous and mucosal blistering and scarring associated with severe deformities and major extracutaneous involvement.

SEVERE GENERALIZED RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA Is also known as rdeb, hallopeau-siemens type|severe generalized rdeb|dystrophic epidermolysis bullosa, autosomal recessive|rdeb generalisata gravis|epidermolysis bullosa dystrophica, hallopeau-siemens type|rdeb-sev gen|autosomal recessive dystrophic epidermolysis bullosa

Related symptoms:

  • Growth delay
  • Neoplasm
  • Cataract
  • Anemia
  • Flexion contracture


SOURCES: ORPHANET OMIM MENDELIAN

More info about SEVERE GENERALIZED RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA

High match FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1


Familial adenomatous polyposis-1 is an autosomal dominant disorder characterized by predisposition to cancer. Affected individuals usually develop hundreds to thousands of adenomatous polyps of the colon and rectum, a small proportion of which will progress to colorectal carcinoma if not surgically treated. Gardner syndrome is a variant of FAP in which desmoid tumors, osteomas, and other neoplasms occur together with multiple adenomas of the colon and rectum (Nishisho et al., 1991).Rustgi (2007) reviewed the genetics of hereditary colon cancer, including APC. Genetic Heterogeneity of Familial Adenomatous PolyposisSee also autosomal recessive FAP2 (OMIM ), caused by mutation in the MUTYH gene (OMIM ) on chromosome 1p34; autosomal recessive FAP3 (OMIM ), caused by mutation in the NTHL1 gene (OMIM ) on chromosome 16p13; and autosomal recessive FAP4 (OMIM ), caused by mutation in the MSH3 gene (OMIM ) on chromosome 5q11.

FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1 Is also known as apc|familial polyposis of the colon|fpc|adenomatous polyposis of the colon|polyposis, adenomatous intestinal

Related symptoms:

  • Intellectual disability
  • Neoplasm
  • Abnormality of the dentition
  • Kyphoscoliosis
  • Carcinoma


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL ADENOMATOUS POLYPOSIS 1; FAP1

High match MUTILATING PALMOPLANTAR KERATODERMA WITH PERIORIFICIAL KERATOTIC PLAQUES


Mutilating palmoplantar keratoderma (PPK) with periorificial keratotic plaques (also known as Olmsted syndrome) is a hereditary palmoplantar keratoderma characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques.

MUTILATING PALMOPLANTAR KERATODERMA WITH PERIORIFICIAL KERATOTIC PLAQUES Is also known as palmoplantar and periorificial keratoderma|mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques|olms|olmsted syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Growth delay


SOURCES: ORPHANET OMIM MENDELIAN

More info about MUTILATING PALMOPLANTAR KERATODERMA WITH PERIORIFICIAL KERATOTIC PLAQUES

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 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

Top 5 symptoms//phenotypes associated to Carcinoma and Carious teeth

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Nail dystrophy Common - Between 50% and 80% cases
Squamous cell carcinoma Common - Between 50% and 80% cases
Alopecia Uncommon - Between 30% and 50% cases
Abnormality of the dentition Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Carcinoma and Carious teeth. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Neoplasm of the skin Intellectual disability Nail dysplasia Palmoplantar keratoderma Erythema Hyperkeratosis Hyperhidrosis Flexion contracture Papule Osteolysis Melanoma Hearing impairment Scaling skin Esophageal stricture Scarring Pruritus Syndactyly Oral leukoplakia Conjunctivitis Pain Periodontitis Osteoporosis Corneal erosion Telangiectasia Ichthyosis

Rare Symptoms - Less than 30% cases


Atypical scarring of skin Recurrent skin infections Delayed skeletal maturation Sparse hair Abnormality of the fingernails Corneal opacity Hypotrichosis Inflammatory abnormality of the skin Keratitis Thickened skin Skin ulcer Elbow flexion contracture Kyphoscoliosis Amniotic constriction ring Abnormality of the tongue Palmoplantar hyperkeratosis Premature loss of primary teeth Gingivitis Progressive visual loss Atrophic scars Milia Ectropion Squamous cell carcinoma of the skin Ankyloglossia Abnormal blistering of the skin Corneal scarring Abnormality of the anus Fragile skin Neoplasm of the lung Visual loss Dysphagia Sensorineural hearing impairment Anemia Growth delay Plantar hyperkeratosis Dermal atrophy Skin vesicle Ridged nail Abnormality of skin pigmentation Hypoplasia of dental enamel Cellulitis Poikiloderma Hyperpigmentation of the skin Sparse eyelashes Arthritis Basal cell carcinoma Breast carcinoma Onycholysis Opacification of the corneal stroma Pili torti Mutism Anhidrosis Curly hair Parakeratosis Epidermal acanthosis Ankylosis Cutis laxa Generalized osteoporosis Hypergranulosis Hidrotic ectodermal dysplasia Skin fissure Circumungual hyperkeratosis Agenesis of premolar Ainhum Foot pain Autoamputation Palmoplantar hyperhidrosis Subungual hyperkeratosis Abnormality of the gingiva Abnormal oral mucosa morphology Abnormal cornea morphology Alopecia universalis Convex nasal ridge Trichorrhexis nodosa Ectodermal dysplasia Verrucae Hypodontia Absent gallbladder Fibroadenoma of the breast Cholangiocarcinoma Colorectal polyposis Multiple impacted teeth Adrenocortical carcinoma Intestinal polyp Chondrosarcoma Abdominal mass Thoracic kyphoscoliosis Keloids Hepatoblastoma Papillary thyroid carcinoma Epidermoid cyst Adrenocortical adenoma Osteoma Multiple gastric polyps Camptodactyly of finger Global developmental delay Thin nail Patchy alopecia Joint laxity Severe short stature Onychomycosis Sebaceous gland carcinoma Seizures Unerupted tooth Congenital hypertrophy of retinal pigment epithelium Duodenal polyposis Desmoid tumors Small intestine carcinoid Duodenal adenocarcinoma Odontoma Adenomatous colonic polyposis Anal fissure Dry skin Finger syndactyly Sparse and thin eyebrow Hypoplastic toenails Absent eyebrow Congenital sensorineural hearing impairment Urticaria Reduced tendon reflexes Knee flexion contracture Hypohidrosis Aplasia/Hypoplasia of the eyebrow Aganglionic megacolon Fine hair Delayed eruption of teeth Severe global developmental delay Photophobia Pes cavus Hemiplegia/hemiparesis Macule Blindness Recurrent corneal erosions Trichiasis Moderate hearing impairment Corneal ulceration Generalized hyperkeratosis Recurrent bacterial skin infections Keratoconjunctivitis Corneal neovascularization Severe hearing impairment Dystrophic fingernails Hypoplastic fingernail Furrowed tongue Dystrophic toenail Abnormal eyelash morphology Alopecia of scalp Keratoconjunctivitis sicca Cerebellar hypoplasia Visual impairment Glioma Colitis Esophagitis Abnormality of the skull Turricephaly Gingival bleeding Cutaneous finger syndactyly Aplasia/Hypoplasia of the skin Inflammation of the large intestine Short 4th metacarpal Abnormality of the hand Abnormality of dental enamel Cutaneous photosensitivity Abnormality of the ribs Eczema Hypopigmentation of the skin Abnormal toenail morphology Short 5th metacarpal Cryptorchidism Symblepharon Short stature Neoplasm of the urethra Telangiectases in sun-exposed and nonexposed skin Acral blistering Diffuse skin atrophy Overjet Severe photosensitivity Cheilitis Spotty hyperpigmentation Phimosis Spotty hypopigmentation Urethral stricture Laryngeal stenosis Eczematoid dermatitis Overbite Stomach cancer Astrocytoma Medulloblastoma Limited elbow extension Cold-induced sweating Unexplained fevers Excessive salivation Trismus Thoracolumbar scoliosis Renal cell carcinoma Opisthotonus Recurrent bacterial infections 2-3 toe syndactyly Radial deviation of finger Cubitus valgus Recurrent upper respiratory tract infections Poor suck Abnormal autonomic nervous system physiology Recurrent respiratory infections Meningitis Sensorimotor neuropathy Otitis media Reduced number of teeth Respiratory tract infection Neutropenia Lymphoma Hypopigmented skin patches Decreased antibody level in blood Generalized hirsutism Sinusitis Abnormality of the nail Hypertrichosis Cerebral calcification Recurrent urinary tract infections Arachnodactyly Bronchiectasis Leukocytosis Lumbar hyperlordosis Premature loss of teeth Bone marrow hypercellularity Low-set ears B-cell lymphoma Muscle weakness Micrognathia Scoliosis Myelokathexis Hypersegmentation of neutrophil nuclei High palate Tonsillitis Septic arthritis Folliculitis Abnormality of bone marrow cell morphology Abnormality of female external genitalia Abnormality of female internal genitalia IgG deficiency Feeding difficulties Round face Apnea Full cheeks Abnormality of the foot Protruding ear Hyperlordosis Feeding difficulties in infancy Camptodactyly Facial palsy Depressed nasal bridge Combined immunodeficiency Osteomyelitis Clinodactyly Long philtrum Anteverted nares Peripheral neuropathy Sparse body hair Pustule Intestinal polyposis Absent fingernail Intellectual disability, moderate Spontaneous esophageal perforation Mitten deformity Esophageal stenosis Loss of eyelashes Refractory anemia Thrombocytopenia Infertility Absent toenail Scarring alopecia of scalp Cirrhosis Microdontia Pancytopenia Small nail Leukemia Horseshoe kidney Sparse scalp hair Multiple lipomas Thyroid carcinoma Atelectasis Brain neoplasm Increased circulating cortisol level Microcephaly Increased number of teeth Neurofibromas Hyperextensible skin Agenesis of permanent teeth Chorioretinal atrophy Colon cancer Intestinal obstruction Precocious puberty Sarcoma Blepharitis Hepatic fibrosis Respiratory failure Choroid plexus calcification Cataract Congestive heart failure Atrophy of alveolar ridges Halitosis Chronic furunculosis Severe periodontitis Recurrent cutaneous abscess formation Pterygium of nails Cigarette-paper scars Liver abscess Immunodeficiency Pneumonia Stomatitis Fragile nails Fever Cardiomyopathy Bone marrow hypocellularity Aplastic anemia Malnutrition Hypoalbuminemia Pterygium Epiphora Joint contracture of the hand Pulmonary fibrosis Delayed puberty Decreased mean platelet volume Toe syndactyly Dilated cardiomyopathy Nasolacrimal duct obstruction Osteopenia Narrow mouth Constipation Abnormality of corneal stroma



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