Melanoma, and Migraine

Diseases related with Melanoma and Migraine

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

Top matches:

Blackfan-Diamond anemia (DBA) is a congenital aregenerative and often macrocytic anemia with erythroblastopenia.

BLACKFAN-DIAMOND ANEMIA Is also known as congenital hypoplastic anemia, blackfan-diamond type|congenital pure red cell aplasia|aase-smith syndrome ii|congenital prca|aase-smith ii syndrome|aase syndrome

Related symptoms:

  • Short stature
  • Growth delay
  • Hypertelorism
  • Neoplasm
  • Failure to thrive


SOURCES: ORPHANET OMIM MENDELIAN

More info about BLACKFAN-DIAMOND ANEMIA

Anaplastic oligoastrocytoma is a rare and aggressive glial tumor of the central nervous system, that usually presents in adults with seizures, is most often located in the cerebral hemispheres and that is associated with a very poor prognosis.

ANAPLASTIC OLIGOASTROCYTOMA Is also known as amoa

Related symptoms:

  • Seizures
  • Neoplasm
  • Headache
  • Brain neoplasm
  • Glioma


SOURCES: ORPHANET MENDELIAN

More info about ANAPLASTIC OLIGOASTROCYTOMA

Low match COWDEN SYNDROME

Cowden syndrome (CS) is a difficult to recognize, under-diagnosed genodermatosis characterized by the presence of multiple hamartomas in various tissues and an increased risk for malignancies of the breast, thyroid, endometrium, kidney and colorectum. When CS is accompanied by germline PTEN mutations, it belongs to the PTEN hamartoma tumor syndrome (PHTS; see this term) group.

COWDEN SYNDROME Is also known as bzs|cowden disease|bbrs|macrocephaly, multiple lipomas, and hemangiomata|pten hamartoma tumor syndrome with granular cell tumor|bannayan-zonana syndrome|macrocephaly, pseudopapilledema, and multiple hemangiomata|cs|cd|mham|pten hamartoma tumor syndrome|ri

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: ORPHANET OMIM MENDELIAN

More info about COWDEN SYNDROME

Other less relevant matches:

Both familial and sporadic pituitary adenomas have been found to be caused by germline mutation in the CDH23 gene. Familial pituitary adenoma types include growth hormone (GH)-secreting and nonfunctional tumors. Sporadic pituitary adenoma types include GH-secreting, nonfunctional, prolactin (PRL)-secreting, adrenocorticotropin (ACTH)-secreting, thyroid-stimulating hormone (TSH)-secreting, and plurihormonal (GH and TSH) tumors.For a general description and a discussion of genetic heterogeneity of pituitary adenomas, see PITA1 (OMIM ).

Related symptoms:

  • Neoplasm
  • Headache
  • Pituitary adenoma


SOURCES: OMIM MENDELIAN

More info about PITUITARY ADENOMA 5, MULTIPLE TYPES; PITA5

Neurofibromatosis type 2 (NF2) is a tumor-prone disorder characterized by the development of multiple schwannomas and meningiomas.

NEUROFIBROMATOSIS TYPE 2 Is also known as nf2|bilateral acoustic neurofibromatosis|central neurofibromatosis

Related symptoms:

  • Ataxia
  • Sensorineural hearing impairment
  • Cataract
  • Visual impairment
  • Gait disturbance


SOURCES: ORPHANET MENDELIAN

More info about NEUROFIBROMATOSIS TYPE 2

Leber's hereditary optic neuropathy (LHON) is a mitochondrial neurodegenerative disease affecting the optic nerve and often characterized by sudden vision loss in young adult carriers.

LEBER HEREDITARY OPTIC NEUROPATHY Is also known as leber optic atrophy|lhon|leber hereditary optic neuropathy

Related symptoms:

  • Ataxia
  • Visual impairment
  • Peripheral neuropathy
  • Optic atrophy
  • Tremor


SOURCES: OMIM ORPHANET MENDELIAN

More info about LEBER HEREDITARY OPTIC NEUROPATHY

Malignant melanoma is a neoplasm of pigment-producing cells called melanocytes that occurs most often in the skin, but may also occur in the eyes, ears, gastrointestinal tract, leptomeninges, and oral and genital mucous membranes (summary by Habif, 2010).For a discussion of genetic heterogeneity of malignant melanoma, see {155600}.

Related symptoms:

  • Neoplasm
  • Melanoma


SOURCES: OMIM MENDELIAN

More info about MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5; CMM5

Malignant melanoma is a neoplasm of pigment-producing cells called melanocytes that occurs most often in the skin, but may also occur in the eyes, ears, gastrointestinal tract, leptomeninges, and oral and genital mucous membranes (summary by Habif, 2010).For a discussion of genetic heterogeneity of cutaneous malignant melanoma, see {155600}.

Related symptoms:

  • Neoplasm
  • Melanoma


SOURCES: OMIM MENDELIAN

More info about MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6; CMM6

Vestibular schwannoma is a rare tumor of the posterior fossa originating in the Schwann cells of the vestibular transitional zone of the vestibulocochlear nerve that can be benign, small, slow growing and asymptomatic or large, faster growing and aggressive and potentially fatal, presenting with symptoms of hearing and balance impairment, vertigo, ataxia, headache and fifth, sixth or seventh cranial nerve dysfunction and facial numbness.

VESTIBULAR SCHWANNOMA Is also known as bilateral acoustic neurofibromatosis|acoustic neurilemoma|acoustic schwannomas, bilateral|banf|neurofibromatosis, central type|acoustic neurinoma|acn|acoustic neuroma|acoustic neurinoma, bilateral

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Neoplasm
  • Sensorineural hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about VESTIBULAR SCHWANNOMA

Top 5 symptoms//phenotypes associated to Melanoma and Migraine

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Headache Uncommon - Between 30% and 50% cases
Ataxia Uncommon - Between 30% and 50% cases
Neoplasm of the skin Uncommon - Between 30% and 50% cases
Subcutaneous nodule Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Melanoma and Migraine. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Meningioma Visual impairment Cataract Papule Neoplasm of the central nervous system Astrocytoma Multiple cafe-au-lait spots Increased intracranial pressure Seizures

Rare Symptoms - Less than 30% cases

Gait disturbance Muscle weakness Pain Hearing impairment Cranial nerve paralysis Sensorineural hearing impairment Vertigo Facial palsy Dysgraphia Reduced visual acuity Blindness Peripheral neuropathy Progressive visual loss Occasional neurofibromas Pseudoepiphyses of the metacarpals Abnormality of the retinal vasculature Cafe-au-lait spot Myopathy Tinnitus Sensory neuropathy Tremor Telangiectasia Visual loss Corneal opacity Incoordination Short stature Hamartoma Hypertelorism Failure to thrive Autism Micrognathia Arrhythmia Papilledema Atrial septal defect Pseudopapilledema Trichilemmoma Abnormality of the penis Subcutaneous lipoma Colonic diverticula Adenoma sebaceum Generalized hyperkeratosis Decreased proportion of CD4-positive T cells Benign neoplasm of the central nervous system Fibroma Hamartomatous polyposis Optic atrophy Behavioral abnormality Dystonia Angioid streaks of the fundus Intestinal polyp Ovarian carcinoma Pituitary adenoma Conjunctival hamartoma Ductal carcinoma in situ Cutis marmorata telangiectatica congenita Fibroadenoma of the breast Neoplasm of the thyroid gland Merkel cell skin cancer Multiple trichilemmomata Lobular carcinoma in situ Transitional cell carcinoma of the bladder Enlarged cerebellum Acrokeratosis Mucosal telangiectasiae Progressive macrocephaly Colorectal polyposis Endometrial carcinoma Follicular thyroid carcinoma Varicocele Thyroid adenoma Dysplastic gangliocytoma of the cerebellum Amblyopia Myoclonus Posterior subcapsular cataract Centrocecal scotoma Marcus Gunn pupil Central retinal vessel vascular tortuosity Abnormality of head blood vessel Reduced OCT-measured macular thickness Paralysis Generalized muscle weakness Sensorimotor neuropathy Progressive hearing impairment Oral-pharyngeal dysphagia Neurofibromas Axonal loss Subcapsular cataract Schwannoma Plethora Lisch nodules Cortical cataract Epiretinal membrane Ependymoma Spinal cord tumor Decreased corneal sensation Vestibular Schwannoma Neuroma Retinal hamartoma Mononeuropathy Bilateral vestibular Schwannoma Peripheral Schwannoma Unilateral vestibular Schwannoma Juvenile posterior subcapsular lenticular opacities Vitritis Mitochondrial respiratory chain defects Gait ataxia Optic neuropathy Abnormality of the nervous system Abnormality of movement Confusion Polyneuropathy Optic disc pallor Enlarged polycystic ovaries Vasculitis Atrioventricular block Abnormal electroretinogram Abnormality of mitochondrial metabolism Postural tremor Constriction of peripheral visual field Blurred vision Scotoma Central scotoma Retinal telangiectasia Abnormality of visual evoked potentials Increased reactive oxygen species production Dyschromatopsia Osteosarcoma Wolff-Parkinson-White syndrome Leber optic atrophy Neuritis Retinal vascular tortuosity Abnormality of the optic disc Vascular tortuosity Optic neuritis Ventricular preexcitation Slow decrease in visual acuity Giant somatosensory evoked potentials Papilloma Abnormality of the vasculature Cavernous hemangioma Cognitive impairment Increased mean corpuscular volume Cleft soft palate Reticulocytopenia Fetal distress Persistence of hemoglobin F Brain neoplasm Glioma Intellectual disability Global developmental delay Generalized hypotonia Scoliosis Low-set ears High palate Acute leukemia Delayed speech and language development Motor delay Brachydactyly Myopia Skeletal muscle atrophy Macrocephaly Downslanted palpebral fissures Frontal bossing Hydrocephalus Diarrhea Intellectual disability, mild Kyphosis Immunodeficiency Esophagitis Tracheomalacia Recurrent infections Delayed puberty Cleft palate Anemia Intrauterine growth retardation Fatigue Ventricular septal defect Short nose Patent ductus arteriosus Osteoporosis Retrognathia Cleft lip Pallor Autistic behavior Cleft upper lip Macrocytic anemia Neutropenia Bifid uvula Tetralogy of Fallot Mitral valve prolapse Ventricular hypertrophy Thick lower lip vermilion Depressed nasal ridge Mitral regurgitation Abnormality of the genital system Short thumb Abnormality of the urinary system Abnormality of the hand Triphalangeal thumb Dilatation Pectus excavatum Long penis Hashimoto thyroiditis Cutis marmorata Macule Abnormality of the thyroid gland Multiple lipomas Cystic hygroma Cellulitis Acute myeloid leukemia Hyperthyroidism Ovarian neoplasm Thyroiditis Hodgkin lymphoma Renal cell carcinoma Scaphocephaly Hand polydactyly Lipoma Growth delay Prolactin excess Skin tags Megalencephaly Hydrocele testis Arteriovenous malformation Furrowed tongue Abnormality of the uterus Ovarian cyst Intestinal polyposis Bone cyst Cellular immunodeficiency Melanocytic nevus Intracranial hemorrhage Narrow mouth Lymphoma Hypothyroidism Proximal muscle weakness Carcinoma Intellectual disability, moderate Abnormality of the kidney Leukemia Nausea and vomiting Joint hypermobility Polymicrogyria Palmoplantar keratoderma Hypoplasia of the maxilla Abnormal cerebellum morphology Macroglossia Decreased antibody level in blood Dysdiadochokinesis Overgrowth Intention tremor Broad thumb Chronic diarrhea Exotropia Gynecomastia Lymphopenia Drooling Hemangioma Hypopigmented skin patches Breast carcinoma Goiter Palmoplantar hyperkeratosis Capsular cataract


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