Hypoplasia
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Focal Dermal Hypoplasia Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: Focal dermal hypoplasia (FDH) is an uncommon genetic disorder characterized by distinctive skin abnormalities and a wide variety of defects that affect the eyes; teeth; and skeletal, urinary, gastrointestinal, cardiovascular, and central nervous systems. It is ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 8:28 pm By:
Focal dermal hypoplasia is an uncommon genetic disorder characterized by skin abnormalities and a variety of defects.http://bit.ly/cJo3ay
A novel syndrome of mandibular hypoplasia, deafnes... [J Clin Endocrinol Metab. 2010] - PubMed result
ncbi.nlm.nih.gov — “PubMed is a service of the U.S. National Library of Medicine that includes over 19 million citations from MEDLINE and other life science journals for biomedical articles back to the 1950s. PubMed includes links to full text articles and other related resources.” View full resource at ncbi.nlm.nih.gov
Most Recently Shared on November 16, 2010 at 11:59 am By:
Dr. Aaron Rogers Surgeon, ENT Doctor, Physician, Active Health Library, and Doctor
PubMed: A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystroph... http://bit.ly/9025Hf
Thumb Reconstruction: eMedicine Orthopedic Surgery
emedicine.medscape.com — “Overview: The thumb plays an important role in hand function. Daily tasks involving pinch, grip, grasp, and precision handling are more easily accomplished with an opposable thumb. Traumatic loss, congenital absence, or hypoplasia diminishes or eliminates the thumb's ...” View full resource at emedicine.medscape.com
Most Recently Shared on March 29, 2010 at 4:19 pm By:
Medscape Orthopedics Health Site
Thumb Reconstruction: With an avulsed/amputated thumb, toe-to-hand transfer may need to be considered. http://bit.ly/aEhmSA
Asplenia: eMedicine Pediatrics: General Medicine
emedicine.medscape.com — “Overview: Absent or defective splenic function is associated with a high risk of fulminant bacterial infections, especially with encapsulated bacteria. Asplenia and splenic hypoplasia are terms used to indicate complete or partial lack of splenic tissue. Loss ...” View full resource at emedicine.medscape.com
Most Recently Shared on August 4, 2010 at 9:47 pm By:
Potter Syndrome: eMedicine Pediatrics: General Medicine
emedicine.medscape.com — “Overview: Potter syndrome refers to the typical physical appearance and associated pulmonary hypoplasia of a neonate as a direct result of oligohydramnios and compression while in utero. The term was coined after the pathologist Edith Potter, who ...” View full resource at emedicine.medscape.com
Most Recently Shared on July 30, 2010 at 8:10 pm By:
Medscape Pediatrics Pediatrics and Health Site
Potter Syndrome: http://bit.ly/c8oWZT
DiGeorge Syndrome: eMedicine Dermatology
emedicine.medscape.com — “Overview: DiGeorge anomaly is one of a group of disorders that share a chromosome deletion resulting in monosomy 22q11. These disorders include cardiac defect, abnormal face, thymic hypoplasia, cleft palate, and hypocalcemia (CATCH-22) syndrome3, 4; conotruncal ...” View full resource at emedicine.medscape.com
Most Recently Shared on April 21, 2010 at 7:29 pm By:
Susan Scroggins Health Advocate and Active Health Library
DiGeorge syndrome is a congenital defect whose symptoms can vary greatly in those affected. Learn more about it. http://bit.ly/aoVRQV
Animal Model Sheds Light On Rare Genetic Disorder, Major Signaling Pathway
medicalnewstoday.com — “A team of researchers from the University of Utah and Brigham Young University has developed a mouse model of focal dermal hypoplasia, a rare human birth defect that causes serious skin abnormalit” View full resource at medicalnewstoday.com
Most Recently Shared on July 21, 2011 at 12:05 pm By:
Animal Model Sheds Light On Rare Genetic Disorder, Major Signaling Pathway http://mnt.to/3YqF #genetics
[Pena-Shokeir syndrome type I - combination of pol... [Orv Hetil. 2010] - PubMed result
ncbi.nlm.nih.gov — “PubMed is a service of the U.S. National Library of Medicine that includes over 19 million citations from MEDLINE and other life science journals for biomedical articles back to the 1950s. PubMed includes links to full text articles and other related resources.” View full resource at ncbi.nlm.nih.gov
Most Recently Shared on June 5, 2010 at 6:42 pm By:
[Pena-Shokeir syndrome type I - combination of polyhydramnios and pulmonary hypoplasia in fetal akinesia.]: We pre... http://bit.ly/9e9UaE
Impairment of the tRNA splicing endonuclease subun... [Hum Mol Genet. 2011] - PubMed result
ncbi.nlm.nih.gov — “PubMed is a service of the U.S. National Library of Medicine that includes over 19 million citations from MEDLINE and other life science journals for biomedical articles back to the 1950s. PubMed includes links to full text articles and other related resources.” View full resource at ncbi.nlm.nih.gov
Most Recently Shared on February 3, 2011 at 11:01 pm By:
Jon D. Moulton PhD, Active Health Library, Doctor, and Science Enthusiast
Impairing tsen54 gene causes neuro abnormalities & larval death in zebrafish models of Pontocerebellar Hypoplasia. http://bit.ly/gx9gID
Poland symdrome ~ Diagnosis of Poland Syndrome
realself.com — “Poland syndrome is mammary hypoplasia (small breast) in association with an upper exptremity anomally which is typically absence of the pectoralis major...” View full resource at realself.com
Most Recently Shared on February 11, 2011 at 7:52 am By:
Helping Animals Through Social Media | The Wandering Duck Climbs a Mountain
ehilpipre.wordpress.com — “Helping Animals Through Social Media | The Wandering Duck Climbs a Mountain” View full resource at ehilpipre.wordpress.com
Most Recently Shared on November 12, 2011 at 10:29 pm By:
RT @NEHumaneSociety: Its early in #Blogpocalypse & @ehilpipre is using words like Cerebellar Hypoplasia http://t.co/GLHtcqhV #blogpocalypse
Animal Model Sheds Light on Rare Genetic Disorder, Major Signaling Pathway
newswise.com — “A team of researchers from the University of Utah and Brigham Young University has developed a mouse model of focal dermal hypoplasia, a rare human birth defect that causes serious skin abnormalities and other medical problems. This animal model not only provides insight into studying the cause of focal dermal hypoplasia (FDH), but also offers a novel way to study a signaling pathway that is crucial for embryonic development.” View full resource at newswise.com
Most Recently Shared on July 20, 2011 at 6:28 pm By:
#health news: Animal Model Sheds Light on Rare Genetic Disorder, Major Signaling Pathway: A team of researchers ... http://bit.ly/mTNtor
Researchers develop mouse model of rare human birth defect
news-medical.net — “A team of researchers from the University of Utah and Brigham Young University has developed a mouse model of focal dermal hypoplasia, a rare human birth defect that causes serious skin abnormalities and other medical problems. This animal model not only provides insight into studying the cause of focal dermal hypoplasia (FDH), but also offers a novel way to study a signaling pathway that is crucial for embryonic development.” View full resource at news-medical.net
Most Recently Shared on July 21, 2011 at 9:52 am By:
Genetics News: Researchers develop mouse model of rare human birth defect: A team of researchers from the Univer... http://bit.ly/r6kA9e
Symposier - Agenic Kidney
symposier.com — “Uploaded and Shared in Youtube by: NationwideChildrens Renal hypoplasia, dysplasia, and aplasia refer to conditions in which the kidneys do not form correctly while a baby is in the womb. Combined, these conditions occur in 2-4% of the population. These conditions are the most common cause of kidney failure in children, although many children do not have any problems from these conditions and go undiagnosed. Renal aplasia occurs when the kidney does not form at all. Renal hypoplasia occurs when ” View full resource at symposier.com
Most Recently Shared on February 2, 2011 at 5:46 pm By:
Symposier Nephrology Health Business and Nephrology
Agenic Kidney Animation. http://bit.ly/93Mdmp
Animal model sheds light on rare genetic disorder, signaling pathway
medicalxpress.com — “A team of researchers from the University of Utah and Brigham Young University has developed a mouse model of focal dermal hypoplasia, a rare human birth defect that causes serious skin abnormalities and other medical problems. This animal model not only provides insight into studying the cause of focal ...” View full resource at medicalxpress.com
Most Recently Shared on July 20, 2011 at 6:13 pm By:
PhysOrg Health News Health News
Animal model sheds light on rare genetic disorder, signaling pathway http://tw.medicalxpress.com/230390023
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Susan S
Mom working in health content publishing field. Enjoy sharing information for healthy living.
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Dr. Aaron Rogers
Dr. Aaron Rogers completed medical school at the University of South Florida with Honors in Research and Alpha Omega Alpha distinctions. Subsequently Dr. Rogers was selected to attend the Emory University residency in Otolaryngology in Atlanta. After finishing a general surgery internship in 2006, the next four years were spent completing the Otolaryngology - Head & Neck Surgery training program. His final year at Emory was spent as Chief Resident for the department.
Dr. Rogers is a member of the American Academy of Otolaryngology - Head & Neck Surgery, the American Academy of Otolaryngic Allergy, and the Georgia Society of Otolaryngology. His professional interests include treatments of nasal and sinus conditions, endoscopic skull base procedures, endoscopic voice surgery, neck and throat lesions, and general ear, nose and throat disorders.
Dr. Rogers has written several scientific publications, editor of a nationally-distributed pocket guide for ENT trainees, and authored a chapter in the textbook Skullbase Surgery Techniques and Concepts. Additionally he has presented medical research at many recent leading national scientific conferences. -
Medscape Orthopedics
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