What is Oppositional Defiant Disorder (ODD) - Symptoms & Statistics

What is Oppositional Defiant Disorder (ODD) - Symptoms & Statistics

Blog: PTEN Gene for Concerned Parents... There is so much to tell!  Cameron is 3 years, 3 months old and he is a smart boy!  Cam has been said to have PTEN Macrocephaly Autism:  a mutation of his PTEN gene, which is from what I understand the tumor suppressor gene.  To me, this means that without proper function of the gene, cells can grow quickly - both good cells and bad cells. http://ptenparents.blogspot.co.uk/. Last blog post: 02.2013

Blog: PTEN Gene for Concerned Parents... There is so much to tell! Cameron is 3 years, 3 months old and he is a smart boy! Cam has been said to have PTEN Macrocephaly Autism: a mutation of his PTEN gene, which is from what I understand the tumor suppressor gene. To me, this means that without proper function of the gene, cells can grow quickly - both good cells and bad cells. http://ptenparents.blogspot.co.uk/. Last blog post: 02.2013

Mutations of the PTEN gene have long been linked with cancer. Recently, however, researchers at the Cleveland Clinic have found that PTEN mutations are found in a small subgroup (about 1-2%) of children who have autism.

Clinic research on rare type of autism linked to PTEN gene reveals potential clues to the brain disorder

Mutations of the PTEN gene have long been linked with cancer. Recently, however, researchers at the Cleveland Clinic have found that PTEN mutations are found in a small subgroup (about 1-2%) of children who have autism.

Paediatric inflammatory bowel diseases (IBD):  The researchers targeted the PTEN gene ... “No one thought that PTEN was associated with IBD,” Dr. Rhee says. “But we hypothesized that it might have something to do with the pathogenesis because the intestinal epithelial cell needs to be readily proliferated to maintain the integrity of the intestine, and the key factor controlling this cell proliferation is the PTEN gene.” gastro.ucla.edu workfiles newsletters BTSFall2014Final.pdf

Paediatric inflammatory bowel diseases (IBD): The researchers targeted the PTEN gene ... “No one thought that PTEN was associated with IBD,” Dr. Rhee says. “But we hypothesized that it might have something to do with the pathogenesis because the intestinal epithelial cell needs to be readily proliferated to maintain the integrity of the intestine, and the key factor controlling this cell proliferation is the PTEN gene.” gastro.ucla.edu workfiles newsletters BTSFall2014Final.pdf

How to Turn on Cancer Fighting Genes: Dr Nalini Chilkov. Here is a list of plant medicines that contain constituents that may talk to your PTEN gene and turn it on, get it activated or prevent damage and malformation (mutation) of the PTEN gene. • Quercetin...      • Resveratrol... • Genistein and Daedzein...     • Curcumin...    • Honokiol... http://www.huffingtonpost.com/nalini-chilkov/how-to-turn-on-a-gene-tha_b_926755.html

How to Turn on Cancer Fighting Genes: Dr Nalini Chilkov. Here is a list of plant medicines that contain constituents that may talk to your PTEN gene and turn it on, get it activated or prevent damage and malformation (mutation) of the PTEN gene. • Quercetin... • Resveratrol... • Genistein and Daedzein... • Curcumin... • Honokiol... http://www.huffingtonpost.com/nalini-chilkov/how-to-turn-on-a-gene-tha_b_926755.html

The+Dual+Life+of+PTEN:+Gene+Mutations+Contribute+to+Both+Cancer+and+Birth+Defects

The Dual Life of PTEN: Gene Mutations Contribute to Both Cancer and Birth Defects

The+Dual+Life+of+PTEN:+Gene+Mutations+Contribute+to+Both+Cancer+and+Birth+Defects

An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy...  CS has been rarely reported in association with a cortical malformation or epilepsy... These cases suggest that cortical dysplasia needs to be suspected when a CS patient presents with drug-resistant seizures.    http://www.brainanddevelopment.com/article/S0387-7604(12)00070-8/abstract  Image…

An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy... CS has been rarely reported in association with a cortical malformation or epilepsy... These cases suggest that cortical dysplasia needs to be suspected when a CS patient presents with drug-resistant seizures. http://www.brainanddevelopment.com/article/S0387-7604(12)00070-8/abstract Image…

A novel PTEN gene promoter mutation and untypical Cowden syndrome: A 72-year-old woman was admitted...for an investigation of her personal history of multiple neoplasms:   breast... colon... and thyroid...http://www.thecjcr.org/article/view/2205/3060. Image: http://www.cam.ac.uk/research/news/novel-genetic-mutations-cause-low-metabolic-rate-and-obesity

A novel PTEN gene promoter mutation and untypical Cowden syndrome: A 72-year-old woman was admitted...for an investigation of her personal history of multiple neoplasms: breast... colon... and thyroid...http://www.thecjcr.org/article/view/2205/3060. Image: http://www.cam.ac.uk/research/news/novel-genetic-mutations-cause-low-metabolic-rate-and-obesity

Dermoscopy of Cowden syndrome.. 'We describe 4 patients with known mutations in the PTEN gene (OMIM 158350) to illustrate the use of dermoscopy and the histologic appearance of palmar lesions in Cowden syndrome.' http://archderm.jamanetwork.com/article.aspx?articleid=711998

Dermoscopy of Cowden syndrome.. 'We describe 4 patients with known mutations in the PTEN gene (OMIM 158350) to illustrate the use of dermoscopy and the histologic appearance of palmar lesions in Cowden syndrome.' http://archderm.jamanetwork.com/article.aspx?articleid=711998

Bannayan Ruvalcaba Riley Syndrome (PTEN gene mutation): Usually diagnosed early in life. Symptoms may include macrocephaly, lipomatosis, hemangiomas, pigmented macules of the penis, high birth weight, proximal myopathy, joint hyperextensibility, pectus excavatum, scoliosis, developmental delay.... Intestinal polyposis is seen in up to 45% of patients predominantly in the distal ileum and colon... http://acgcasereports.gi.org/2014/01/10/bannayan-ruvalcaba-riley-syndrome/. Linked with autism.

Bannayan Ruvalcaba Riley Syndrome (PTEN gene mutation): Usually diagnosed early in life. Symptoms may include macrocephaly, lipomatosis, hemangiomas, pigmented macules of the penis, high birth weight, proximal myopathy, joint hyperextensibility, pectus excavatum, scoliosis, developmental delay.... Intestinal polyposis is seen in up to 45% of patients predominantly in the distal ileum and colon... http://acgcasereports.gi.org/2014/01/10/bannayan-ruvalcaba-riley-syndrome/. Linked with autism.

Cowden's/ Bannayan Riliey Ruvalcaba syndrome.   My husband and I discovered that our young son (now 34 months) had a PTEN gene mutation. He had undergone genetic testing to try to establish if there was a cause of his developmental delay, macrocephaly (large head) and autistic behaviour. http://hannahjanelee.wordpress.com/tag/cowden-syndrome/

Cowden's/ Bannayan Riliey Ruvalcaba syndrome. My husband and I discovered that our young son (now 34 months) had a PTEN gene mutation. He had undergone genetic testing to try to establish if there was a cause of his developmental delay, macrocephaly (large head) and autistic behaviour. http://hannahjanelee.wordpress.com/tag/cowden-syndrome/

Cowden's syndrome/BRRS. Each PTEN gene mutation case is different. Nathaniel does not have autism, down-slanted eyes, or... He has two tiny skin-colored bumps on his fingers (acral keratoses), these would go unnoticed by most people... he had hundreds of polyps in his small intestine... I had inquired about seeking a genetics evaluation several times, but each time I was told that it was probably not necessary. http://ptenlife.com/nathaniels-story/

Cowden's syndrome/BRRS. Each PTEN gene mutation case is different. Nathaniel does not have autism, down-slanted eyes, or... He has two tiny skin-colored bumps on his fingers (acral keratoses), these would go unnoticed by most people... he had hundreds of polyps in his small intestine... I had inquired about seeking a genetics evaluation several times, but each time I was told that it was probably not necessary. http://ptenlife.com/nathaniels-story/

Muscle Hemangiomatosis Presenting as a Severe Feature in a Patient with the PTEN Mutation... This case report reminds the clinicians to consider a PTEN gene mutation testing for diagnosis of patients with vascular anomalies. http://www.bjmg.edu.mk/UploadedImages/pdf/46-51.pdf. Image: and other clinical features of CS and BRRS.

Muscle Hemangiomatosis Presenting as a Severe Feature in a Patient with the PTEN Mutation... This case report reminds the clinicians to consider a PTEN gene mutation testing for diagnosis of patients with vascular anomalies. http://www.bjmg.edu.mk/UploadedImages/pdf/46-51.pdf. Image: and other clinical features of CS and BRRS.

When Emma was about a year we had been noticing things didn’t come so easy for her. She wasn’t as far developmentally as she should have been...the doctor diagnosed autism... we had lots of bloodwork done  and it came back that Emma had a PTEN gene mutation.  http://ptenlife.com/emmas-story/

When Emma was about a year we had been noticing things didn’t come so easy for her. She wasn’t as far developmentally as she should have been...the doctor diagnosed autism... we had lots of bloodwork done and it came back that Emma had a PTEN gene mutation. http://ptenlife.com/emmas-story/

Researchers have now collected enough rare mutations associated with autism to begin finding patterns of common disrupted pathways and networks.

Researchers have now collected enough rare mutations associated with autism to begin finding patterns of common disrupted pathways and networks.

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