17q12, uitgelegd voor kinderendeletion syndrome · static snapshot
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Gen + lichaamsdeel Hoe het eruit kan zien 5 ondersteunende bronnen vertrouwen 97% nieuwheid 54%

Het gen ACACA wordt in 5 verhalen genoemd samen met ogen, oren en gehoor

We lazen 5 verhalen die het over zowel het gen ACACA als over ogen, oren en gehoor hebben. Dat betekent niet zeker dat het één het ander veroorzaakt, maar het komt wel vaak samen voor.

Hoe dit tot stand kwam

Dit gaat over wat er samen in de artikelen staat. Het is geen bewijs dat het ene het andere veroorzaakt.

Gegenereerd 2026-11-13, laatst gewijzigd gisteren. Dedup-sleutel assoc:ACACA:sensory. De engine controleert dit inzicht bij elke analyse opnieuw; als meer bronnen het eens zijn, stijgen zijn onderbouwing en vertrouwen en verschijnt het opnieuw als “nieuw”.

Bewijs (4 citaten)

…]. Diabetes mellitus is typically the first manifestation, often presenting in the first decade of life, followed by optic atrophy and sensorineural hearing loss. The neurodegeneration observed in these patients mirrors the β-cell destruction, as neurons are also highly dependent on proper ER and mitochondrial…
…rome (XLAS) (OMIM 301050) [ 9 ]. The phenotype is variable and includes progressive renal failure due to glomerulopathy associated with sensorineural hearing loss (SNHL) and ocular anomalies [ 96 ]. Impaired hearing is frequently detectable by late childhood or early adolescence in boys with XLAS. SNHL develops…
…270), an autosomal recessive disorder caused by mutations in the SLC19A2 gene. It is characterized by megaloblastic anemia, progressive sensorineural hearing loss, and diabetes with age of onset from infancy to adolescence [ 33 ]. The so-called Mitchell-Riley syndrome (OMIM #615710), another rare syndromic form…
…s. In myosin heavy chain 9 ( MYH9 )-related disease, hematuria can coexist with congenital macrothrombocytopenia and later proteinuria, sensorineural hearing loss, cataracts, or elevated liver enzymes [ 21 , 22 ]. Automated analyzers may underestimate platelet count and size because giant platelets are not reco…

Ondersteunende documenten (38)

VerhaalBronGepubliceerdGezienRelevantie
Ten tips for ordering, interpreting, and communicating genetic test... pmc 2026-01-01 gisteren 1.00
17q12 Recurrent Deletion Syndrome in Childhood pmc 2025-01-01 gisteren 1.00
Genetics of CAKUT pmc 2026-01-01 gisteren 1.00
HNF1β, LHX1, and GGNBP2 deletion contributed to kidney and reproduc... pmc 2024-01-01 gisteren 1.00
Prenatal diagnosis of 17q12 copy number variants in fetuses via chr... pmc 2024-01-01 gisteren 1.00
Monogenic Defects of Beta Cell Function: From Clinical Suspicion to... pmc 2024-01-01 gisteren 0.45
HNF1B Transcription Factor: Key Regulator in Renal Physiology and P... pmc 2024-01-01 gisteren 1.00
A Case of Diabetes Mellitus Type MODY5 as a Feature of 17q12 Deleti... pmc 2024-01-01 gisteren 1.00
Prenatal diagnosis of familial transmission of 17q12 microduplicati... pubmed 2016-12-01 gisteren 1.00
Semaglutide as a potential therapeutic alternative for HNF1B-MODY: ... pubmed 2024-01-01 gisteren 1.00
Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advance... pubmed 2024-01-01 gisteren 1.00
HNF1B-MODY (MODY-5): a rare form of diabetes with multisystemic fea... pubmed 2026-01-01 gisteren 1.00
Delineation of the Genetic Architecture and Clinical Polymorphism o... pmc 2024-01-01 gisteren 1.00
Identification and functional analysis of a novel SMARCC2 splicing ... pmc 2025-01-01 gisteren 1.00
Decreased T helper 1 cell function underlies recurrent sinopulmonar... pmc 2025-01-01 gisteren 1.00
Case-based learning: a case of maturity-onset diabetes of the young... pmc 2025-01-01 gisteren 1.00
Navigating Genetic Testing in Nephrology: Options and Decision-Maki... pmc 2024-01-01 gisteren 1.00
Severe neonatal cholestasis in HNF1β deficiency: a case report and ... pmc 2025-01-01 gisteren 1.00
Exome analysis links kidney malformations to developmental disorder... pmc 2025-01-01 gisteren 1.00
Diabetes associated with HNF1B: beyond Occam’s razor—A case report pmc 2025-01-01 gisteren 1.00
Persistent Tic Disorders Are Associated With 17q12 Duplications pmc 2025-01-01 gisteren 1.00
A Case of Amyotrophic Lateral Sclerosis With Coexisting Maturity-on... pmc 2025-01-01 gisteren 1.00
MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Pren... pmc 2025-01-01 gisteren 1.00
Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebell... pmc 2025-01-01 gisteren 1.00
Unexpected genomic architecture in a sporadic case of C1-INH Heredi... pmc 2025-01-01 gisteren 1.00
Reversed cortico-medullary differentiation in kidneys on fetal magn... pmc 2025-01-01 gisteren 1.00
The Genetic Landscape and Precision Medicine in Neonatal Diabetes M... pmc 2026-01-01 gisteren 1.00
Genetic testing in chronic kidney disease of uneXplained cause (CKD... pmc 2026-01-01 gisteren 1.00
The Importance of Molecular Testing in the Diagnosis of Genetic Syn... pmc 2026-01-01 gisteren 1.00
Transient neonatal diabetes mellitus as an early diagnostic clue to... pmc 2026-01-01 gisteren 1.00
Functional validation of a non-canonical HNF1B splice-site variant in MODY5 pmc 2026-01-01 gisteren 1.00
17q12 deletion syndrome presenting with chronic pancreatitis: a case report pmc 2026-01-01 gisteren 1.00
A familial case report of 17q12 recurrent deletion syndrome: clinic... pmc 2026-01-01 gisteren 1.00
A phenome-wide association study of CNVs genotyped from genome sequ... pmc 2026-01-01 gisteren 1.00
Multiple-testing corrections in selection scans using identity-by-d... pmc 2025-01-01 gisteren 1.00
The population frequency of predicted pathogenic genetic variants i... pmc 2026-01-01 gisteren 1.00
Precision Medicine in Pediatric Nephrology: From Shared Clinical Ph... pmc 2026-01-01 gisteren 1.00
Case-based learning: a case of maturity-onset diabetes of the young... pubmed 2025-04-01 gisteren 1.00