Carcinoma, and Delayed eruption of teeth

Diseases related with Carcinoma and Delayed eruption of teeth

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


Top matches:

High match PAPILLOMA OF CHOROID PLEXUS; CPP


Choroid plexus tumors are of neuroectodermal origin and range from benign choroid plexus papillomas (CPPs) to malignant choroid carcinomas (CPCs). These rare tumors generally occur in childhood, but have also been reported in adults. Patients typically present with signs and symptoms of increased intracranial pressure including headache, hydrocephalus, papilledema, nausea, vomiting, cranial nerve deficits, gait impairment, and seizures (summary by Safaee et al., 2013).

PAPILLOMA OF CHOROID PLEXUS; CPP Is also known as choroid plexus papilloma

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hypertelorism
  • Neoplasm
  • Abnormal facial shape


SOURCES: OMIM MENDELIAN

More info about PAPILLOMA OF CHOROID PLEXUS; CPP

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

High match HUTCHINSON-GILFORD PROGERIA SYNDROME


Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat).

HUTCHINSON-GILFORD PROGERIA SYNDROME Is also known as progeria|hgps

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Scoliosis
  • Growth delay


SOURCES: OMIM ORPHANET MENDELIAN

More info about HUTCHINSON-GILFORD PROGERIA SYNDROME

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Other less relevant matches:

Medium 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

Medium match SOTOS SYNDROME 1; SOTOS1


SOTOS SYNDROME 1; SOTOS1 Is also known as chromosome 5q35 deletion syndrome|sotos syndrome|cerebral gigantism

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: OMIM MENDELIAN

More info about SOTOS SYNDROME 1; SOTOS1

Medium match BASAL CELL NEVUS SYNDROME; BCNS


BASAL CELL NEVUS SYNDROME; BCNS Is also known as nevoid basal cell carcinoma syndrome|gorlin-goltz syndrome|gorlin syndrome|nbccs|multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Microcephaly
  • Scoliosis
  • Ataxia


SOURCES: OMIM MENDELIAN

More info about BASAL CELL NEVUS SYNDROME; BCNS

Low 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

Low match DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6


Dyskeratosis congenita is a multisystem disorder caused by defective telomere maintenance. Features are variable and include bone marrow failure, nail dysplasia, oral leukoplakia, and increased risk of cancer (summary by Kocak et al., 2014).For a discussion of genetic heterogeneity of dyskeratosis congenita, see DKCA1 (OMIM ).

Related symptoms:

  • Global developmental delay
  • Microcephaly
  • Growth delay
  • Neoplasm
  • Anemia


SOURCES: OMIM MENDELIAN

More info about DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6; DKCA6

Low match COLORECTAL CANCER; CRC


Colorectal cancer is a heterogeneous disease that is common in both men and women. In addition to lifestyle and environmental risk factors, gene defects can contribute to an inherited predisposition to CRC. CRC is caused by changes in different molecular pathogenic pathways, such as chromosomal instability, CpG island methylator phenotype, and microsatellite instability. Chromosome instability is the most common alteration and is present in almost 85% of all cases (review by Schweiger et al., 2013). Genetic Heterogeneity of Colorectal CancerMutations in a single gene result in a marked predisposition to colorectal cancer in 2 distinct syndromes: familial adenomatous polyposis (FAP ) and hereditary nonpolyposis colorectal cancer (HNPCC; see {120435}). FAP is caused by mutations in the APC gene (OMIM ), whereas HNPCC is caused by mutations in several genes, including MSH2 (OMIM ), MLH1 (OMIM ), PMS1 (OMIM ), PMS2 (OMIM ), MSH6 (OMIM ), TGFBR2 (OMIM ), and MLH3 (OMIM ). Epigenetic silencing of MSH2 results in a form of HNPCC (see HNPCC8, {613244}). Other colorectal cancer syndromes include autosomal recessive adenomatous polyposis (OMIM ), which is caused by mutations in the MUTYH gene (OMIM ), and oligodontia-colorectal cancer syndrome (OMIM ), which is caused by mutations in the AXIN2 gene (OMIM ).The CHEK2 gene (OMIM ) has been implicated in susceptibility to colorectal cancer in Finnish patients. A germline mutation in the PLA2G2A gene (OMIM ) was identified in a patient with colorectal cancer.Germline susceptibility loci for colorectal cancer have also been identified. CRCS1 (OMIM ) is conferred by mutation in the GALNT12 gene (OMIM ) on chromosome 9q22; CRCS2 (OMIM ) maps to chromosome 8q24; CRCS3 (OMIM ) is conferred by variation in the SMAD7 gene (OMIM ) on chromosome 18; CRCS4 (OMIM ) is conferred by variation on 15q that causes increased and ectopic expression of the GREM1 gene (OMIM ); CRCS5 (OMIM ) maps to chromosome 10p14; CRCS6 (OMIM ) maps to chromosome 8q23; CRCS7 (OMIM ) maps to chromosome 11q23; CRCS8 (OMIM ) maps to chromosome 14q22; CRCS9 (OMIM ) maps to 16q22; CRCS10 (OMIM ) is conferred by mutation in the POLD1 gene (OMIM ) on chromosome 19q13; CRCS11 (OMIM ) maps to chromosome 20p12; and CRCS12 (OMIM ) is conferred by mutation in the POLE gene (OMIM ) on chromosome 12q24.Somatic mutations in many different genes, including KRAS (OMIM ), PIK3CA (OMIM ), BRAF (OMIM ), CTNNB1 (OMIM ), FGFR3 (OMIM ), AXIN2 (OMIM ), AKT1 (OMIM ), MCC (OMIM ), MYH11 (OMIM ), PARK2 (OMIM ), and RNF43 (OMIM ), have been identified in colorectal cancer.

COLORECTAL CANCER; CRC Is also known as colon cancer

Related symptoms:

  • Neoplasm
  • Carcinoma
  • Oligodontia
  • Colon cancer
  • Colitis


SOURCES: OMIM MENDELIAN

More info about COLORECTAL CANCER; CRC

Low match SCHÖPF-SCHULZ-PASSARGE SYNDROME


Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.

SCHÖPF-SCHULZ-PASSARGE SYNDROME Is also known as palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome|keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis|eccrine tumors with ectodermal dysplasia|ssps|palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypot

Related symptoms:

  • Neoplasm
  • Alopecia
  • Hyperhidrosis
  • Hyperkeratosis
  • Carcinoma


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about SCHÖPF-SCHULZ-PASSARGE SYNDROME

Top 5 symptoms//phenotypes associated to Carcinoma and Delayed eruption of teeth

Symptoms // Phenotype % cases
Neoplasm Very Common - Between 80% and 100% cases
Intellectual disability Common - Between 50% and 80% cases
Abnormality of the dentition Uncommon - Between 30% and 50% cases
Carious teeth Uncommon - Between 30% and 50% cases
Cryptorchidism Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Alopecia Hearing impairment Abnormal facial shape Sparse hair Palmoplantar keratoderma Nail dysplasia Hypertelorism Neoplasm of the skin Pain Thin nail Squamous cell carcinoma Basal cell carcinoma Nail dystrophy Agenesis of permanent teeth Scoliosis Hypotrichosis Macrocephaly Renal cell carcinoma Abnormality of the skeletal system Hypodontia

Rare Symptoms - Less than 30% cases


Relative macrocephaly Infertility Osteolysis Parietal bossing Mandibular prognathia Fragile nails Bird-like facies Sparse and thin eyebrow Coarse facial features Frontal bossing Convex nasal ridge Downslanted palpebral fissures Hamartomatous polyposis Hypohidrosis Conductive hearing impairment Hypermetropia Hypogonadotrophic hypogonadism Cataract Micrognathia Growth delay Prominent forehead Hypoplasia of dental enamel Proptosis Colitis Down-sloping shoulders Oral leukoplakia Alopecia of scalp Keratoconjunctivitis sicca Ulcerative colitis Aplasia/Hypoplasia of the eyebrow Macrotia Small nail Microcephaly Colon cancer Sensorineural hearing impairment Brain neoplasm Astrocytoma Precocious puberty Midface retrusion Medulloblastoma Global developmental delay Hyperpigmentation of the skin Leukemia Kyphoscoliosis Atrial septal defect Short stature Hydrocephalus Multiple impacted teeth Colorectal polyposis Strabismus Hyperhidrosis Visual loss Hyperkeratosis Ridged nail Cerebellar hypoplasia Seizures Onycholysis Prolonged neonatal jaundice Fibroadenoma of the breast Partial agenesis of the corpus callosum Osteoma Large hands Small cell lung carcinoma Nephroblastoma Redundant skin Acute lymphoblastic leukemia Reduced number of teeth Abnormality of the cerebral ventricles Cutis laxa Abnormal dermatoglyphics Accelerated skeletal maturation Neuroblastoma Long foot Poor coordination Abdominal mass Adrenocortical carcinoma Overbite Abnormal glucose tolerance Hyperplasia of the maxilla Expressive language delay Periventricular leukomalacia Oxycephaly Sacrococcygeal teratoma High anterior hairline Gray matter heterotopias Cavum septum pellucidum Advanced eruption of teeth Cholangiocarcinoma Intestinal polyp Teratoma Enlarged cisterna magna Narrow palate Optic atrophy Pointed chin Jaundice Genu valgum Dolichocephaly Respiratory tract infection Generalized hypotonia Abnormality of the kidney Joint laxity Ataxia Neonatal hypotonia Pes planus High, narrow palate Nystagmus Abnormal heart morphology Patent ductus arteriosus Behavioral abnormality Ventriculomegaly Ventricular septal defect High palate Delayed speech and language development Joint hypermobility Vesicoureteral reflux Multiple gastric polyps Tall stature Unerupted tooth Adenomatous colonic polyposis Odontoma Narrow face Duodenal adenocarcinoma Hyperreflexia Abnormal vertebral morphology Lymphedema Small intestine carcinoid Otitis media Heterotopia Clumsiness Desmoid tumors Duodenal polyposis Apraxia Sloping forehead Overgrowth Renal agenesis Congenital hypertrophy of retinal pigment epithelium Aggressive behavior Arachnodactyly Cleft palate Cardiac rhabdomyoma Onychomycosis Patchy alopecia Breast carcinoma Telangiectasia Hamartomatous stomach polyps Irregular ossification of hand bones Cardiac fibroma Bridged sella turcica Plantar pits Ovarian fibroma Odontogenic keratocysts of the jaw Bifid ribs Anemia Curved fingers Histiocytoma Calcification of falx cerebri Orbital cyst Palmar pits Short distal phalanx of the thumb Severe hydrocephalus Ovarian carcinoma Vertebral wedging Abnormality of the sense of smell Fibroma Sebaceous gland carcinoma Intrauterine growth retardation Supernumerary ribs Abnormality of the eye Apocrine hidrocystoma Narrow nail Abnormality of primary teeth Trichodysplasia Facial telangiectasia Plantar hyperkeratosis Toenail dysplasia Premature loss of primary teeth Ovarian neoplasm Palmoplantar hyperkeratosis Ectodermal dysplasia Uterine leiomyosarcoma Pancytopenia Neoplasm of the stomach Hereditary nonpolyposis colorectal carcinoma Transitional cell carcinoma of the bladder Endometrial carcinoma Leiomyosarcoma Retinoblastoma Oligodontia Esophageal stenosis Esophageal stricture Aplastic anemia Bone marrow hypocellularity Cervical ribs Ectopic calcification Spasticity Retrognathia Iris coloboma Oral cleft Cleft upper lip Chondrosarcoma Papule Coloboma Facial palsy Cleft lip Telecanthus Proteinuria EEG abnormality Polydactyly Nevus Glaucoma Abdominal pain Brachycephaly Pectus excavatum Microphthalmia Syndactyly Wide nasal bridge Brachydactyly Dysarthria Epicanthus Motor delay Postaxial polydactyly Hypotension Broad face Disproportionate tall stature Neoplasm of the endocrine system Abnormality of the neck Short 4th metacarpal Skin tags Narrow nose Sprengel anomaly Thoracic scoliosis Abnormality of the sternum Vertebral fusion Long fingers Milia Inflammation of the large intestine Cerebral calcification Melanocytic nevus Nephritis Glomerulonephritis Spina bifida occulta Hemivertebrae Muscle stiffness Short ribs Spina bifida Bradycardia Exotropia Hemiparesis Abnormality of the ribs Absent gallbladder Regional abnormality of skin Thoracic kyphoscoliosis Corneal neovascularization Trichiasis Moderate hearing impairment Corneal ulceration Generalized hyperkeratosis Recurrent bacterial skin infections Corneal scarring Keratoconjunctivitis Squamous cell carcinoma of the skin Abnormality of the tongue Recurrent corneal erosions Dystrophic fingernails Failure to thrive Hypoplastic fingernail Furrowed tongue Dystrophic toenail Corneal erosion Abnormal eyelash morphology Severe hearing impairment Cellulitis Macule Hemiplegia/hemiparesis Hypoplastic toenails Abnormality of corneal stroma Flexion contracture Keratitis Hypertrophic cardiomyopathy Chest pain Hepatic steatosis Thin vermilion border Delayed puberty Narrow chest Dilated cardiomyopathy Hip dislocation Microtia Stroke Joint stiffness Osteopenia Hypertension Dyspnea Narrow mouth Hypogonadism Osteoporosis Dementia Malar flattening Short nose Kyphosis Congestive heart failure Cardiomyopathy Skeletal muscle atrophy Absent eyebrow Congenital sensorineural hearing impairment Growth hormone deficiency Hydronephrosis Broad neck Papilledema Upper limb undergrowth Loss of consciousness Increased intracranial pressure Sleep apnea Hypertrichosis Macroglossia Nausea Apnea High forehead Broad ribs Micropenis Respiratory failure Pneumonia Depressivity Recurrent infections Headache Vomiting Talipes equinovarus Feeding difficulties Low-set ears Choanal stenosis Osteosarcoma Scaling skin Progressive visual loss Urticaria Reduced tendon reflexes Sparse eyelashes Conjunctivitis Knee flexion contracture Elbow flexion contracture Skin ulcer Thickened skin Aganglionic megacolon Fine hair Ichthyosis Papilloma Severe global developmental delay Scarring Erythema Arthritis Photophobia Pes cavus Delayed skeletal maturation Blindness Visual impairment Choroid plexus carcinoma Choroid plexus papilloma Limitation of joint mobility Cyanosis Keloids Sinus tachycardia Bilateral coxa valga Craniofacial disproportion Old-aged sensorineural hearing impairment Reticulated skin pigmentation Hypoplastic facial bones Prominent scalp veins Mitral valve calcification Widely patent fontanelles and sutures Intermittent claudication Corneal arcus Decreased testosterone in males Carotid artery stenosis Premature coronary artery atherosclerosis Absence of subcutaneous fat Hip pain Aplastic clavicle Narrow nasal ridge Arteriosclerosis Carcinoid tumor Prolonged prothrombin time Decreased serum estradiol Thin bony cortex Narrow nasal tip Absence of pubertal development Precocious atherosclerosis Increased number of teeth Hepatoblastoma Papillary thyroid carcinoma Epidermoid cyst Adrenocortical adenoma Stomach cancer Glioma Intestinal polyposis Thyroid carcinoma Increased circulating cortisol level Neoplasm of the lung Multiple lipomas Insulin-resistant diabetes mellitus at puberty Neurofibromas Chorioretinal atrophy Intestinal obstruction Sarcoma Hyperextensible skin Melanoma Horseshoe kidney Intellectual disability, moderate Tapering pointed ends of distal finger phalanges Arteriosclerosis of small cerebral arteries Abnormal trabecular bone morphology Enlarged joints Aplasia/Hypoplasia of the earlobes Abnormality of the cardiovascular system Increased bone mineral density Intracranial hemorrhage Nasal speech Dermal atrophy Hypercholesterolemia Acanthosis nigricans Hyperlipidemia Atherosclerosis Aminoaciduria Coxa valga Hypergonadotropic hypogonadism Aspiration Hyperinsulinemia Aortic valve stenosis Insulin resistance Dental crowding Left ventricular hypertrophy Decreased body weight Broad-based gait Thin skin Osteoarthritis Hypertriglyceridemia Myocardial infarction Cardiomegaly Lipodystrophy Premature ovarian insufficiency Small face Thrombocytosis Generalized osteoporosis Lack of skin elasticity Angina pectoris Prominent superficial veins Osteolytic defects of the phalanges of the hand Ovoid vertebral bodies Hyperphosphatemia Transient ischemic attack Absent eyelashes Abnormal EKG Short clavicles Metaphyseal widening Hypoplastic nipples Thin ribs Scleroderma Lipoatrophy Exertional dyspnea Prolonged QT interval Premature graying of hair High pitched voice Multiple joint contractures Heart murmur Abnormality of the thorax Poroma



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Dysarthria and Abnormality of the metaphysis, related diseases and genetic alterations Neuroblastoma and Paralysis, related diseases and genetic alterations Delayed speech and language development and Coarctation of aorta, related diseases and genetic alterations Muscle weakness and Syncope, related diseases and genetic alterations Scoliosis and Talipes equinovarus, related diseases and genetic alterations Muscular hypotonia and Dandy-Walker malformation, related diseases and genetic alterations Scoliosis and Full cheeks, related diseases and genetic alterations

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