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861 Possible Causes for Aniridia, Neuroblastoma

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  • Nephroblastoma

    Postoperative renal function was unimpaired in 4 patients and 1 patient had Wilms tumor/aniridia/genitourinary malformations/retardation syndrome with glomerulopathy.[] Neuroblastoma (NBL) is the most common extra-cranial tumour in childhood.[] Wilms' tumor occurs more frequently in children with certain abnormalities or syndromes present at birth, including: Aniridia.[]

  • Beckwith-Wiedemann Syndrome

    Disability Syndrome; Aniridia - Renal Agenesis - Psychomotor Retardation; Aniridia - Ptosis - Intellectual Disability - Familial Obesity; Aniridia - Cerebellar Ataxia - Intellectual[] We report the case of a newborn with Beckwith-Wiedemann syndrome presenting the simultaneous occurrence of a cystic pancreatoblastoma and an adrenal neuroblastoma.[] […] present the case of an infant with BWS who has hypomethylation of LIT1 gene in the 11p15.5 chromosomal region and at 6 months of age presented with simultaneous occurrence of neuroblastoma[]

  • Multiple Endocrine Neoplasia Type 2A

    Disability Syndrome; Aniridia - Renal Agenesis - Psychomotor Retardation; Aniridia - Ptosis - Intellectual Disability - Familial Obesity; Aniridia - Cerebellar Ataxia - Intellectual[] The diagnostic problems of this tumor after basic tests were between neuroblastoma and medullary thyroid carcinoma.[] Iobenguane I 123 (Brand name: Adreview ) - Manufactured by GE Healthcare, Inc FDA-approved indication: To be used in the detection of primary or metastatic pheochromocytomas or neuroblastomas[]

  • Gonadoblastoma

    Another three aniridia/gonablastoma observations from the literature are discussed, two of them without and one in combination with Wilms' tumor.[] ORPHA:1642 Synonym(s): Distal deletion Simpson Golabi Behmel syndrome (Wilms tumor (see this term), hepatoblastoma, adrenal neuroblastoma, gonadoblastoma, hepatocellular carcinoma[] An incidence of bilateral gonadoblastoma in a 23-month old, mentally retarded boy with congenital sporadic aniridia, undescended dysgenetic testes, deletion of a chromosome[]

  • Clear Cell Sarcoma

    […] and due to several distinctive features has been classified separately from Wilms tumour. [1] Unlike Wilms tumour it is not associated with hemihypertrophy and sporadic aniridia[] To our knowledge, this may be the first case of synchronous CCSK and differentiating neuroblastoma being reported.[] Most Ewing sarcomas and all neuroblastomas showed diffuse moderate to strong staining.[]

  • Anisocoria

    Hemmorage Multiple sclerosis Retinal Disease Tuberculosis Trauma Neoplastic Ocular prosthesis Syphilis Tapes Dorsalis Keratitis Degenerative Neurologic disorder Syringomyelia Aniridia[] In children, Horner’s syndrome may be caused by neuroblastoma, a tumor arising in another part of the body.[] […] hypoxemic lesions of the Parasympathetic and Orthosympathetic Nervous System. 2 Local causes reported in Literature are synechia, congenital iris disorders (coloboma and aniridia[]

  • Hydrophthalmos

    ( Q10-Q18 , 743-744 ) Eyes eyelid, lacrimal apparatus and orbit (Ptosis, Ectropion, Entropion, Distichia) Anophthalmia - Microphthalmia lens ( Ectopia lentis , Aphakia) Aniridia[] The GLC3B locus identified in this study maps centromeric to Charcot-Marie-Tooth Type 2a ( CMT2A ) and neuroblastoma loci ( 21 , 22 ).[] Other conditions causing buphthalmos: Aniridia: Characterized by complete or partial iris hypoplasia. Inheritance is autosomal dominant.[]

  • Nystagmus

    • Cataract • Strabismus • Amblyopia • Optic nerve hypoplasia • Leber’s congenital amaurosis • Aniridia • Achromatopsia • Severe refractive error • Retina coloboma • Other[] Opsoclonus/Saccadomania Saccadic intrusions with conjugate, multidirectional eye movements have been attributed to viral illness, neuroblastoma (children), and visceral carcinoma[] A rare cancer called neuroblastoma effects the sympathetic nervous system, most commonly found in children. Labyrinthitis is another ear disorder.[]

  • Microdontia

    […] systemic features of Axenfeld-Rieger syndrome may even have typical anterior chamber features of Axenfeld-Rieger anomaly in one eye and severe iris hypoplasia resembling aniridia[] CONCLUSIONS: Chemotherapy on children treated for neuroblastoma can adversely influence tooth development.[] Aim of this case report is to present the late effects of chemotherapy on dental development in a patient treated for neuroblastoma at early age. DESIGN: Case report.[]

  • Familial Acute Necrotizing Encephalopathy

    Anauxetic Dysplasia approved 607095 Anderson Fabry Disease approved 301500 Androgen Insensitivity Syndrome approved 300068 Angelman Syndrome (UBE3A gene only) approved 105830 Aniridia[] Craniopharyngioma Familial isolated dilated cardiomyopathy Hepatocellular carcinoma, childhood-onset Inherited acute myeloid leukemia Jeune syndrome Muscular dystrophy, Selcen type Neuroblastoma[]

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