About ▼ Careers Internship MedBlog Contact us

LOGIN REGISTER

Medindia » Apert Syndrome

Apert Syndrome News, Research and Latest Updates

Keep abreast with the latest news related to Apert Syndrome there are 273 news items on Apert Syndrome that covers updates, breakthroughs and in-depth reports.

We provide you with a free downloadable secure widget for your website to carry news related to Apert Syndrome.

Apert Syndrome

Apert syndrome is a rare inherited condition marked by abnormal shape of the face and skull due to premature fusion of the bones, and webbing of hands and feet.

PARMESAN: New AI Tool Revolutionizing Genetic Disorder Treatments

PARMESAN: New AI Tool Revolutionizing Genetic Disorder Treatments

PARMESAN, the natural language processing tool accelerates research, boosting drug discovery and development for scientists.

Likely Cause of Common Penis Birth Defect Identified

Likely Cause of Common Penis Birth Defect Identified

Tissues samples with mild cases of hypospadias (male birth defect) had a greater degree of epigenetic alterations, revealed study.

Childhood Glaucoma Could be due to a Genetic Mutation

Childhood Glaucoma Could be due to a Genetic Mutation

A new genetic mutation could be the cause of childhood blindness in children as young as 3 years old.

Advertisement

Genetic Mutation can Identify Women With Difficulty Producing Breast Milk: Study

Genetic Mutation can Identify Women With Difficulty Producing Breast Milk: Study

Maternal genetics with nutrients in breast milk can affect the supply of milk while breastfeeding.

Genetic Mutation Puts High-risk Women for Ovarian Cancer

Genetic Mutation Puts High-risk Women for Ovarian Cancer

New study findings hold potential for predicting many years in advance which women with the BRCA-1mutation will develop ovarian cancer.

Repurposed Amyotrophic Lateral Sclerosis (ALS) Drug Against Rare Genetic Disorder

Repurposed Amyotrophic Lateral Sclerosis (ALS) Drug Against Rare Genetic Disorder

Repurposed ALS (amyotrophic lateral sclerosis) drug may help slow down a rare genetic disorder in children and adolescents.

Advertisement

Alzheimer’s Disease With Genetic Mutation Disrupts the Brain’s White Matter

Alzheimer’s Disease With Genetic Mutation Disrupts the Brain’s White Matter

Alzheimer’s disease with genetic mutation disrupts the structural integrity of the brain’s white matter even in cognitively normal individuals.

Cause Of Common Zika Virus Birth Defect Revealed

Cause Of Common Zika Virus Birth Defect Revealed

A new study has identified how Zika virus (ZIKV) causes one of the most common birth defects linked to prenatal infection.

New Genetic Disorder Affects Brain and Craniofacial Skeleton

New Genetic Disorder Affects Brain and Craniofacial Skeleton

Researchers at the National Institutes of Health have discovered a new genetic disorder characterized by developmental delays and malformations of the brain, heart and facial features.

Advertisement

Umbilical Cord Patch for Spinal Bifida Birth Defect

Umbilical Cord Patch for Spinal Bifida Birth Defect

Human umbilical cord patch is used to treat spinal bifida birth defect as it improves healing, reduces scars, it is effective in watertight closure, and regeneration of meningeal layer.

1 2 3 4 5 6 7 8 ..28

Download Apert Syndrome News Widget

Recommended Reading

Novel Method to Evaluate Children With Rare Skull Abnormality

Novel Method to Evaluate Children With Rare Skull Abnormality

A new method to help determine when surgery is needed for children with metopic craniosynostosis has been developed by researchers.

One Gene Linked With Craniosynostosis, Delayed Tooth Eruption and Supernumerary Teeth

One Gene Linked With Craniosynostosis, Delayed Tooth Eruption and Supernumerary Teeth

A new, recessively inherited human syndrome featuring craniosynostosis, maxillary hyperplasia, delayed tooth eruption and extra teeth has been identified by researchers.

Quiz on Genetic Disorders

Quiz on Genetic Disorders

genetic mutations and these mutations may be small, affecting just one gene or affecting entire chromosomes. Such mutations may develop spontaneously or they may be inherited from either parent. The consequences of such genetic disorders can vary ...

Genetic Testing of Diseases

Genetic Testing of Diseases

Genetic testing helps to confirm a genetic condition in an individual and involves q complex laboratory techniques

Stickler Syndrome

Stickler Syndrome

Stickler Syndrome is a rare genetic disorder which causes multisystem disorders predominantly affecting vision, joints, and heart.

Craniosynostosis

Craniosynostosis

Craniosynostosis is a condition where the bones of the skull are fused together prematurely affecting the development of the skull.