Updated: 18 Apr 2024
Newly Posted
- KMT2E-Related Neurodevelopmental Disorder 18 Apr 2024
- Osteoglophonic Dysplasia 18 Apr 2024
- CDKL5 Deficiency Disorder 11 Apr 2024
- DYNC1H1-Related Disorders 21 Mar 2024
- Classic Isovaleric Acidemia 14 Mar 2024
- Schinzel-Giedion Syndrome 07 Mar 2024
Updated
- HFE-Related Hemochromatosis 11 Apr 2024
- CSF1R-Related Disorder 04 Apr 2024
- Geleophysic Dysplasia 28 Mar 2024
- EZH2-Related Overgrowth 21 Mar 2024
- Long QT Syndrome Overview 21 Mar 2024
- Trichorhinophalangeal Syndrome 21 Mar 2024
- Adenosine Deaminase Deficiency 07 Mar 2024
- POLG-Related Disorders 29 Feb 2024
- Hypermobile Ehlers-Danlos Syndrome 22 Feb 2024
- Nevoid Basal Cell Carcinoma Syndrome 22 Feb 2024
- Poikiloderma with Neutropenia 22 Feb 2024
Revised
- Fabry Disease 11 Apr 2024
- Mucopolysaccharidosis Type I 11 Apr 2024
- Mucopolysaccharidosis Type II 11 Apr 2024
- Myotonic Dystrophy Type 1 21 Mar 2024
- COL1A1/2 Osteogenesis Imperfecta 14 Mar 2024
- Von Hippel-Lindau Syndrome 29 Feb 2024
- GLI3-Related Pallister-Hall Syndrome 22 Feb 2024
Updates. Every four to five years (or as needed), a GeneReview entry undergoes a complete, formal review and update in order to maintain currency. Updates are conducted by GeneReviews staff with the participation of the author(s).
Revisions. Whenever a clinically relevant change in information occurs, revisions to a GeneReview entry are initiated by staff or the author(s).
Publication Details
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NLM Citation
Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024. What's New in GeneReviews.