Find information on thousands of medical conditions and prescription drugs.

Angelman syndrome

Angelman syndrome (AS) is neurological disorder in which severe learning difficulties are associated with a characteristic facial appearance and behavior. more...

Home
Diseases
A
Aagenaes syndrome
Aarskog Ose Pande syndrome
Aarskog syndrome
Aase Smith syndrome
Aase syndrome
ABCD syndrome
Abdallat Davis Farrage...
Abdominal aortic aneurysm
Abdominal cystic...
Abdominal defects
Ablutophobia
Absence of Gluteal muscle
Acalvaria
Acanthocheilonemiasis
Acanthocytosis
Acarophobia
Acatalasemia
Accessory pancreas
Achalasia
Achard syndrome
Achard-Thiers syndrome
Acheiropodia
Achondrogenesis
Achondrogenesis type 1A
Achondrogenesis type 1B
Achondroplasia
Achondroplastic dwarfism
Achromatopsia
Acid maltase deficiency
Ackerman syndrome
Acne
Acne rosacea
Acoustic neuroma
Acquired ichthyosis
Acquired syphilis
Acrofacial dysostosis,...
Acromegaly
Acrophobia
Acrospiroma
Actinomycosis
Activated protein C...
Acute febrile...
Acute intermittent porphyria
Acute lymphoblastic leukemia
Acute lymphocytic leukemia
Acute mountain sickness
Acute myelocytic leukemia
Acute myelogenous leukemia
Acute necrotizing...
Acute promyelocytic leukemia
Acute renal failure
Acute respiratory...
Acute tubular necrosis
Adams Nance syndrome
Adams-Oliver syndrome
Addison's disease
Adducted thumb syndrome...
Adenoid cystic carcinoma
Adenoma
Adenomyosis
Adenosine deaminase...
Adenosine monophosphate...
Adie syndrome
Adrenal incidentaloma
Adrenal insufficiency
Adrenocortical carcinoma
Adrenogenital syndrome
Adrenoleukodystrophy
Aerophobia
Agoraphobia
Agrizoophobia
Agyrophobia
Aicardi syndrome
Aichmophobia
AIDS
AIDS Dementia Complex
Ainhum
Albinism
Albright's hereditary...
Albuminurophobia
Alcaptonuria
Alcohol fetopathy
Alcoholic hepatitis
Alcoholic liver cirrhosis
Alektorophobia
Alexander disease
Alien hand syndrome
Alkaptonuria
Alliumphobia
Alopecia
Alopecia areata
Alopecia totalis
Alopecia universalis
Alpers disease
Alpha 1-antitrypsin...
Alpha-mannosidosis
Alport syndrome
Alternating hemiplegia
Alzheimer's disease
Amaurosis
Amblyopia
Ambras syndrome
Amelogenesis imperfecta
Amenorrhea
American trypanosomiasis
Amoebiasis
Amyloidosis
Amyotrophic lateral...
Anaphylaxis
Androgen insensitivity...
Anemia
Anemia, Diamond-Blackfan
Anemia, Pernicious
Anemia, Sideroblastic
Anemophobia
Anencephaly
Aneurysm
Aneurysm
Aneurysm of sinus of...
Angelman syndrome
Anguillulosis
Aniridia
Anisakiasis
Ankylosing spondylitis
Ankylostomiasis
Annular pancreas
Anorchidism
Anorexia nervosa
Anosmia
Anotia
Anthophobia
Anthrax disease
Antiphospholipid syndrome
Antisocial personality...
Antithrombin deficiency,...
Anton's syndrome
Aortic aneurysm
Aortic coarctation
Aortic dissection
Aortic valve stenosis
Apert syndrome
Aphthous stomatitis
Apiphobia
Aplastic anemia
Appendicitis
Apraxia
Arachnoiditis
Argininosuccinate...
Argininosuccinic aciduria
Argyria
Arnold-Chiari malformation
Arrhythmogenic right...
Arteriovenous malformation
Arteritis
Arthritis
Arthritis, Juvenile
Arthrogryposis
Arthrogryposis multiplex...
Asbestosis
Ascariasis
Aseptic meningitis
Asherman's syndrome
Aspartylglycosaminuria
Aspergillosis
Asphyxia neonatorum
Asthenia
Asthenia
Asthenophobia
Asthma
Astrocytoma
Ataxia telangiectasia
Atelectasis
Atelosteogenesis, type II
Atherosclerosis
Athetosis
Atopic Dermatitis
Atrial septal defect
Atrioventricular septal...
Atrophy
Attention Deficit...
Autoimmune hepatitis
Autoimmune...
Automysophobia
Autonomic dysfunction
Familial Alzheimer disease
Senescence
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
Medicines

History

Dr. Harry Angelman, a pediatrician working in Warrington, Cheshire, first reported three children with this condition in 1965. It was initially presumed to be rare. In 1987, it was first noted that around half of the children with Angelman syndrome have a small piece of chromosome 15 missing (chromosome 15q partial deletion). Since this time the condition has been reported more frequently and the incidence is now thought to be 1 in 15,000 children.

Pathophysiology

Angelman syndrome is caused by the loss of the the normal maternal contribution to a region of chromosome 15, most commonly by deletion of a segment of that chromosome. Other causes include uniparental disomy, translocation, or single gene mutation in that region. A healthy person receives two copies of chromosome 15, one from mother, the other from father. However, in the region of the chromosome that is critical for Angelman syndrome, the maternal and paternal contribution express certain genes very differently. This is due to sex-related epigenetic imprinting; the biochemical mechanism is DNA methylation. If the maternal contribution is lost, the result is Angelman syndrome. (When the paternal contribution is lost, by similar mechanisms, the result is Prader-Willi syndrome.)

Angelman syndrome can also be the result of mutation of a single gene. This gene (Ube3a, part of the ubiquitin pathway) is present on both the maternal and paternal chromosomes, but differs in the pattern of methylation (Imprinting). The paternal silencing of the Ube3a gene occurs in a brain region-specific manner; the maternal allele is active almost exclusively in the hippocampus and cerebellum. The most common genetic defect leading to Angelman syndrome is an ~4Mb (mega base) maternal deletion in chromosomal region 15q11-13 causing an absence of Ube3a expression in the maternally imprinted brain regions. Ube3a codes for an E6-AP ubiquitin ligase, which chooses its substrates very selectively and the four identified E6-AP substrates have shed little light on the possible molecular mechanisms underlying the human Angelman syndrome mental retardation state.

Initial studies of mice that do not express maternal Ube3a show severe impairments in hippocampal memory formation. Most notably, there is a deficit in a learning paradigm that involves hippocampus-dependent contextual fear conditioning. In addition, maintenance of long-term synaptic plasticity in hippocampal area CA1 in vitro is disrupted in Ube3a -/- mice. These results provide links amongst hippocampal synaptic plasticity in vitro, formation of hippocampus-dependent memory in vitro, and the molecular pathology of Angelman syndrome.

Read more at Wikipedia.org


[List your site here Free!]


Expert outlines litigation risks related to ART
From OB/GYN News, 2/15/05 by Sherry Boschert

CABO SAN LUCAS, MEXICO -- Higher rates of complications in babies born through assisted reproductive technology have led to malpractice lawsuits, Aubrey Milunsky. M.B., said at a conference on obstetrics, gynecology, perinatal medicine, neonatology, and the law.

"There is a medicolegal industry that is evolving at break-neck speed" related to ART, said Dr. Milunsky, who chaired the conference and is professor of human genetics, pediatrics, ob.gyn., and pathology at Boston University. ART plays a role in approximately 1% of the 4 million births in the United States each year, said Dr. Milunsky, who is also director of the Center for Human Genetics, Boston.

Compared with naturally conceived pregnancies, ART pregnancies carry nearly a threefold increased risk for low birth weight and more than a fivefold increased risk for fetal or infant death. Singletons delivered after ART are 40% more likely to be small for gestational age, 54% more likely to be delivered by cesarean section, and 27% more likely to require intensive care, compared with naturally conceived singletons. Multifetal pregnancies are more common with ART.

Maternal serum screening produces more false-positive results in ART pregnancies than in naturally conceived ones.

The overall rate of birth defects is 40%-200% higher in ART pregnancies than the background rate of 3%-4% in the general population. Three rare "imprinting" birth defects (disorders that appear to develop more in one sex than in the other) have been reported in a handful of ART pregnancies: Beckwith-Wiedemann syndrome, Angelman's syndrome, and retinoblastoma.

When parents have gone to such great lengths to conceive a child through ART and are desperate to have a successful pregnancy, anything less than a "perfect" baby may be extra disappointing, and complications may seem extra burdensome, he added.

Sean Tipton, spokesman for the American Society for Reproductive Medicine in Washington, commented in a subsequent telephone interview, "We're not aware of any explosion in litigation in this area. It's certainly not news to anyone that children of infertility patients are not as healthy as children of healthy people."

Complications in ART pregnancies could be attributed to the underlying cause of the infertility, the advanced age of many women who seek ART, or issues related to multiple gestations, he said.

At the meeting, Dr. Milunsky highlighted some of the key areas for potential litigation related to ART:

* Informed consent. It is difficult and probably rare to get truly informed consent for all stages of ART a patient may go through, such as hormonal therapy, intracytoplasmic sperm injection, manipulation of the gamete or zygote in vitro, or insertion of cells into the womb.

* Extreme prematurity. Birth weights under 2,500 g are 70% more common in ART singletons than in naturally conceived ones. "Even though the technology is so phenomenal in terms of saving them ... the outcome is intellectually disastrous" for many of the extremely small babies, he said. As in non-ART pregnancies, damaged babies lead to lawsuits that often try to pin the blame on medical personnel.

Erroneous diagnosis. Chromosomal testing of a blastomere biopsy can miss problems absent in one cell but present in others. "It's surprising, if not amazing, how often the embryo is made up of two sets of cells--normal and abnormal," he said.

When a fertilized egg multiplies into 8-16 cells in vitro, a gene analysis for cystic fibrosis (CF) typically involves one of those cells. But in some cases allele dropout occurs in the cell chosen for analysis, giving the false impression that the cell--and hence the blastomere--does not contain a CF mutation. At least two lawsuits resulted from missed CF diagnoses due to allele dropout.

* Genetic counseling. Failure to refer both parents for genetic counseling results in inadequate information gathering. "People undergoing ART rarely have a full genetic evaluation, I find," Dr. Milunsky said at the meeting, sponsored by Boston University and the Center for Human Genetics.

* Targeted ultrasound. Given the higher risks for complications in ART pregnancies, targeted ultrasound should be done during the second trimester in all ART pregnancies to search for detectable abnormalities.

* Chorionic villus sampling/amniocentesis. Don't let the parents' drive to succeed in pregnancy keep you from offering invasive testing, which can endanger the pregnancy. Your responsibility is to communicate any increased risk to the parents and give them options for management. "Let them make the choice, and you make the documentation," he said.

BY SHERRY BOSCHERT

San Francisco Bureau

COPYRIGHT 2005 International Medical News Group
COPYRIGHT 2005 Gale Group

Return to Angelman syndrome
Home Contact Resources Exchange Links ebay