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16p11.2p12.2 microduplication syndrome is a rare chromosomal anomaly syndrome resulting from the partial duplication of the short arm of chromosome 16 with a highly variable phenotype typically characterized by developmental/psychomotor delay (particularly of speech), intellectual disability, autism spectrum disorder and/or obsessive and repetitive behavior, behavioral problems (such as aggression and outbursts), dysmorphic facial features (triangular face, deep set eyes, broad and prominent nasal bridge, upslanting or narrow palpebral features, hypertelorism). Additionally, finger/hand anomalies, short stature, microcephaly and slender build are frequently described.
Biomarker and diagnostic research for 16p11.2p12.2 microduplication syndrome has been reported in the published literature.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for 16p11.2p12.2 microduplication syndrome.
100 publications have been identified in PubMed for 16p11.2p12.2 microduplication syndrome. Research spans Case Report / Case Series (34%), Diagnostic / Biomarker (23%), and Review / Meta-Analysis (19%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 34 | 34% |
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 12:02 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Testing and diagnosis research
23 |
23% |
Research summaries | 19 | 19% |
Disease patterns and progression | 10 | 10% |
Laboratory research | 9 | 9% |
Other research | 5 | 5% |
Chen YY (2026). [PMID: 41845159](https://pubmed.ncbi.nlm.nih.gov/41845159/). *World J Pediatr*. [Review / Meta-Analysis]
Choi N (2026). [PMID: 41479269](https://pubmed.ncbi.nlm.nih.gov/41479269/). *J Clin Lab Anal*. [Diagnostic / Biomarker]
De Sousa SMC (2026). [PMID: 41965096](https://pubmed.ncbi.nlm.nih.gov/41965096/). *J Clin Endocrinol Metab*. [Review / Meta-Analysis]
Daly AF (2026). [PMID: 41887597](https://pubmed.ncbi.nlm.nih.gov/41887597/). *Ann Endocrinol (Paris)*. [Other]
Zgheib O (2026). [PMID: 40954079](https://pubmed.ncbi.nlm.nih.gov/40954079/). *Clin Genet*. [Case Report / Case Series]
Xu J (2026). [PMID: 41657460](https://pubmed.ncbi.nlm.nih.gov/41657460/). *Transl Pediatr*. [Case Report / Case Series]
Liu RY (2026). [PMID: 41730779](https://pubmed.ncbi.nlm.nih.gov/41730779/). *Am J Med Genet A*. [Case Report / Case Series]
Kim S (2026). [PMID: 41804817](https://pubmed.ncbi.nlm.nih.gov/41804817/). *Am J Med Genet A*. [Case Report / Case Series]
Zhuang J (2026). [PMID: 41620759](https://pubmed.ncbi.nlm.nih.gov/41620759/). *Hum Genomics*. [Basic Science / Preclinical]
Minale EMP (2026). [PMID: 42003802](https://pubmed.ncbi.nlm.nih.gov/42003802/). *Mol Genet Genomic Med*. [Review / Meta-Analysis]
AI-curated news mentioning 16p11.2p12.2 microduplication syndrome
Updated Aug 25, 2026
The FDA approved Genglycos (pariglasgene brecaparvovec-opnr) to reduce daily cornstarch intake in patients aged 8 years and older with glycogen storage disease type Ia. Known as Von Gierke disease, GSDIa is a rare metabolic disorder caused by a mutation in the G6PC gene. This genetic variation leads to a deficiency in glucose-6-phosphatase (G6Pase), an enzyme needed to release glucose into the bloodstream. Without this enzyme, the body cannot properly maintain blood glucose levels, causing severe hypoglycemia and other serious metabolic complications · Pariglasgene brecaparvovec is an adeno-associated virus (AAV) serotype 8 based gene therapy that delivers a functional copy of the G6PC gene into liver cells, enabling the production of normally functioning G6Pase. Ultragenyx stated that as part of its postmarketing commitments to the FDA, the Company will provide 2 years of clinical data from open-label commercial treatment of 50 patients and 20 control patients through its existing GSDIa Disease Monitoring Program. ... Ultragenyx announces US FDA approval of Genglycos™ gene therapy, the first-ever FDA-approved treatment designed to treat the underlying cause of glycogen storage disease type Ia (GSDIa). “The reduced reliance on cornstarch, experienced by patients in our clinical studies, demonstrates this gene therapy’s ability to establish the normal breakdown of glycogen to produce glucose during fasting or episodes of metabolic stress. This ability to regulate glucose has alleviated the disease burden and has the potential to mitigate the risk of severe or life-threatening hypoglycemia for these patients.” Close more info about First Gene Therapy Approved for Glycogen Storage Disease Type la