Hypotonia
Links shared publicly online about this topic
Hypotonia and Low Tone in Children
nspt4kids.com — “In the pediatric therapy world, a diagnosis --low tone-- or --hypotonia-- is often given. But what exactly does this diagnosis mean for your child?” View full resource at nspt4kids.com
Most Recently Shared on April 24, 2011 at 7:46 pm By:
New blog...: Low Muscle Tone | What Does Hypotonia Mean? http://nspt4kids.com/parenting/low-muscle-tone-what-does-hypotonia-mean/
Teaching NeuroImages: Molar tooth sign with hypotonia, ataxia, and nystagmus (Joubert syndrome) and hypothyroidism --" Neurology
neurology.org — “Teaching NeuroImages: Molar tooth sign with hypotonia, ataxia, and nystagmus (Joubert syndrome) and hypothyroidism --" Neurology” View full resource at neurology.org
Most Recently Shared on December 17, 2009 at 3:33 pm By:
#AAN-Teaching NeuroImage: Molar tooth sign with hypotonia, ataxia, and nystagmus and hypothyroidism http://tinyurl.com/yahtawf
Prader-Willi Syndrome: eMedicine Pediatrics: Genetics and Metabolic Disease
emedicine.medscape.com — “Overview: Prader-Willi syndrome (PWS) is a disorder caused by a deletion or disruption of genes in the proximal arm of chromosome 15 or by maternal disomy in the proximal arm of chromosome 15. Commonly associated characteristics of ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 29, 2009 at 8:42 pm By:
Some new evidence and information added to the Prader-Willi Syndrome eMedicine article. http://bit.ly/dgiLJ #genetics #health #pediatrics
Oculocerebrorenal Dystrophy (Lowe Syndrome): eMedicine Pediatrics: Genetics and Metabolic Disease
emedicine.medscape.com — “Overview: In 1952, Lowe and colleagues described an infant with congenital cataracts and mental retardation. When more patients were described, the phenotype was expanded to include the renal tubular defects that comprise Fanconi syndrome, and an X-linked ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 15, 2009 at 7:45 pm By:
The Lowe Syndrome eMedicine topic has been updated with new information for 2009. http://bit.ly/bWZqq #pediatrics #health #medicine
Partial Trisomy 3p and Partial Monosomy 11q Associated with Atrial Septal Defect, Cleft Palate, and Developmental Delay: A Case Report
content.karger.com — “Unbalanced translocation involving both chromosome 3p duplication and 11q deletion in the same patient is extremely rare; only 1 live-born case was reported previously. This karyotype was also detected during prenatal diagnosis of 2 different pregnancies in a Taiwanese family which were both terminated. In all 3 cases, only standard karyotyping was done to detect the abnormal karyotypes. Here, we report a 4-year-old boy with cleft palate, atrial septal defect, and hypotonia with gross and fine m” View full resource at content.karger.com
Most Recently Shared on June 3, 2011 at 6:42 am By:
Partial Trisomy 3p and Partial Monosomy 11q Associated with Atrial Septal Defect, Cleft Palate, and Developmenta... http://bit.ly/kwtgOU
The Top 3 resources shared on this topic. More resources.
Key stats and trends about this topic
Related WisdomCards
Featuring the top 3 experts for this topic
-
NS Pediatric Therapy
North Shore Pediatric Therapy | Pediatric Blogs, Articles and Parenting Tips by Professionals | 3 locations in Chicagoland
-
Neurology Journal
-
Medscape Pediatrics
Latest medical news, articles, and features from Medscape Pediatrics
Advertisement

