Guest guest Posted March 9, 2002 Report Share Posted March 9, 2002 Hi Leigh! Right off the top I can tell you that Jeannie Buesser -The President of Apraxia Network of Bergan County and Outreach Coordinator for CHERAB has one son with apraxia and ADHD - and a younger son with PDD who is still not talking. You can read her story and much more in the February Exceptional Parent magazine which features an article on verbal apraxia (and CHERAB!) on newstands now. There is more info in the archives on how to get this issue. There are lots of links out there -the best place to search for new ones are at http://www.google.com Once you find the name of a researcher -or University -just put in that name and you'll find more and more. You may want to search under FoxP2 gene for example if you are looking for apraxia and genetic links. Here is what a quick search tonight brought up : A PDF file from Oxford which answers many of your questions about links -genetic included - between ADHD, dyspraxia as well as dyslexia, autism and dysphasia http://www.physiol.ox.ac.uk/~jfs/bioltxt.ppt which has lots of reference as well as to why the PUFA's (like ProEFA or Efalex) are important. Here is an article on speech language impairment (SLI) and genetic links -and anyone with a child with apraxia should also look into and learn about SLI. It's " different " (they say) than apraxia -but it's obvious overlaps happen here as well when you read up on it and " study " your own child with diagnosed apraxia (also you can search much more on SLI -there is a wealth of info on this prevalent speech impairment) http://sls.qmced.ac.uk/talks/Cohen.htm Here is one I found from the US POSTER SESSION 3 S105 Family Pedigrees of Children with Suspected Developmental Apraxia of Speech Barbara Freebairn H. Gerry Deorah V. Dawson Sudha Iyengar Case Western Reserve University Lawrence Shriberg University of Wisconsin - Madison Family pedigrees of a relatively large cohort of children with suspected developmental apraxia of speech (DAS) were examined for familial aggregation. Thirty-eight children (28 males and 10 females) ages 3.08 to 8.8 years, were referred from the caseloads of clinical speech-language pathologists for suspected DAS. DAS was confirmed by examination of developmental history and directly testing speech, language, and oral motor abilities. Family pedigrees were constructed through parent interviews. Twenty-two children (58%) had at least one parent affected suggesting vertical transmission of the disorder and a possible autosomal dominant mode. Mothers (37%) and fathers (32%) were approximately equally affected as were sisters (52%) and brothers (53%). Affection rates of nuclear family members of children with DAS exceeded reported affection rates of nuclear family members of children with phonology disorders. http://www.waisman.wisc.edu/srcld/pages/pastsrclds/2001/abstracts2001/ S1052001.htm And I know that the Neurosciences Lab at Rutgers (the Tallal lab -and Dr. Tallal is one of our advisors) is doing extensive genetic testing on various communication disorders, which perhaps they will answer your excellent question as well as others. I don't believe that there are any experts left who will argue that communication disorders do not overlap. Anyone? ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 18, 2002 Report Share Posted March 18, 2002 Although no one has specifically isolated or identifed an " apraxia gene, " the current finding on FOXP2 on Chromosome 7q suggests that several of the family members in that study had motor speech problems which could be characterized as apraxia. We know that there is often co-morbidity of specific language, speech, and learning problems but having one child with one of these problems does not necessarily mean that other siblings will also present with similar problems. Also, these problems if present are not always of the same intensity. Although I am not familiar with specific rate of apraxia in families, we do know about rates of specific language impairment (SLI) and dyslexia in families. When one person in the family has been identified with either of these problems, the rate of these problems in other family members ranges from aprroximately 20%-40%. There is a person at Case Western Reserve University in Ohio who is working with a team on the genetic basis of apraxia. Her name is Dr. Barbara . When I saw her in November, her analyses were not completed, but she may have more detailed information by now. She would be a good person to contact for more specific information about familial incidence of apraxia and associated conditions. Good luck to you! Judy F. Flax, Ph.D. Center for Molecular and Behavioral Neuroscience Rutgers University 197 University Avenue Newark, New Jersey 07102 (973) 353-1080 x3214 FAX: (973) 353-1760 ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ From: " lbrain123 " <bygpub@...> Date: Fri Mar 8, 2002 4:50 am Subject: Genetic Link to Apraxia? Anyone with 2 affected children in family? My son (4 yrs) has apraxia. My daughter (2 years) does not. Next month I will deliver twin boys and I am wondering how likely they are to have apraxia. Does anyone have 2 or more children in their family (or extended family) with apraxia? Another mother of an apraxic child told me researchers thought it was genetic and also tied to Attention deficit disorder. Are there any families with apraxia and ADD in the same family? My husband's cousin's daughter has also been diagnoised with apraxia which seems like it might point to be genetic. I have seen my son struggle and I hope my twin boys will be spared the same long journey in learning how to speak. But I've never heard of anyone having 2 apraxic children so I wonder if I am worrying over nothing. Anyways, any comments would be appreciated! Thanks! Leigh Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 18, 2002 Report Share Posted March 18, 2002 Thanks Dr. Flax for this answer! Dr. Judy Flax and Dr. a Tallal of the Center for Molecular and Behavioral Neuroscience at Rutgers are two of the advisors for CHERAB. speaking about SLI -here are just two of their many scientific papers about SLI (which also relate to the family question) http://babylab.rutgers.edu/talks/Flax_ASHA2001.pdf http://babylab.rutgers.edu/talks/Flax_IDA2000.pdf ===== Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.