21. HEALTHMEDNET ILLNESS AND DISEASE URL DIRECTORY intrauterine dwarfism (96 sites / 23 books). http//www.e88.com/health_conditions/ .intrauterine dwarfism nord http://www.healthmednet.com/INT-JMS.htm

22. Diagnosis Of Maternal Uniparental Disomy Of Chromosome 7 With A Methylation Spec Russell A. A syndrome of intrauterine dwarfism recognizable at birth withcraniofacial dysostosis, disproportionate short arms and other anomalies. http://jmg.bmjjournals.com/cgi/content/full/37/9/e19

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by KOSAKI, K. Articles by MATSUO, N. Related Collections Genetics J Med Genet e19 ( September ) Electronic letters Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assay E DITOR In approximately 10% of patients with Silver-Russell syndrome, pre- and postnatal growth retardation with relative macrocephaly, triangular facies, and asymmetry is associated with maternal uniparental disomy of chromosome 7 (UPD(7)mat). The purpose of this report is to present a novel assay to diagnose UPD(7)mat by analysing the methylation status of PEG1/MEST , the only known imprinted gene on chromosome 7

23. No Evidence For Mosaicism In Silver-Russell Syndrome -- MONK Et Al. 38 (4): 11 - Russell A. A syndrome of intrauterine dwarfism recognised at birth with craniofacialdysostosis, disproportionate short arms and other anomalies. http://jmg.bmjjournals.com/cgi/content/full/38/4/e11

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by MONK, D. Articles by MOORE, G. E Related Collections Genetics J Med Genet e11 ( April ) Electronic letters No evidence for mosaicism in Silver-Russell syndrome E DITOR Silver-Russell syndrome (SRS) is a condition characterised by pre- and postnatal growth restriction, triangular facies, and limb and truncal asymmetry. The aetiology of the syndrome is heterogeneous and there is no clearly established Mendelian basis. A number of chromosomal abnormalities are associated with the SRS phenotype in a minority of cases. To date, 37 cases of

24. Hill Health Topics A-Z List: I : Health Topics Intrauterine device (IUD) for birth control intrauterine dwarfism Intrauterinefetal blood transfusion for Rh disease Intrauterine Synechiae http://www.healthwise.net/hillhealth/Find/list.aspx?LETTER=I&FILTER=Health Topic

25. All Showcase - Health Disease And Health Conditions Interstitial Cystitis (21). Intestinal Flu (10). Intracranial Hypotension (1).intrauterine dwarfism (4). Iritis (19). Irritable Bowel Syndrome (46) http://www.allshowcase.com/Health_and_Fitness/Conditions_and_Diseases/I/

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26. The World Diseases A 2 Z Names By Countrylinks And Dr Impex intrauterine dwarfism. Iritis. Irritable Bowel Syndrome. J. Jacobsen Syndrome.Jock Itch. Joint Disorders. Joubert Syndrome. Juvenile Rheumatoid Arthritis http://www.countrylinks.biz/diseases.htm

Country Links Dr Impex free on-line Services Note: search with CTRL + F A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease

27. Dubowitz Syndrome 1 Summary, A syndrome of intrauterine dwarfism, short stature, mental retardation,sparse hair, eczema, and characteristic facies. The phenotype varies from http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome272.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome Dubowitz syndrome 1 Synonym dwarfism-eczema-peculiar facies syndrome Summary A syndrome of intrauterine dwarfism, short stature, mental retardation, sparse hair, eczema, and characteristic facies. The phenotype varies from normal growth and head circumference with mild psychomotor retardation and lack of eczema to severe growth and mental retardation, microcephaly, behavioral problems, aplastic anemia, immunological disorders, neoplasms, and eczema Some features of this syndrome are similar to those in Bloom and fetal alcohol syndromes. Major Features Head and neck: Microcephaly, micrognathia, prognathism triangular face, high sloping forehead, craniosynostosis, narrow bifrontal diameter, dolichocephaly, trigonocephaly, small face and narrow face, brachycephaly, large open fontanels, prominent occiput, prominent glabella, flat occiput, and Robin sequence. Ears: Large or small ears, low-set posteriorly angulated ears, hypoplastic helices, anteverted auricles, prominent lower anthelices, folded helices, cup-shaped ears, hypoplastic tragus, and ear or pre-auricular fistulae. Otitis media is frequent. Eyes: Blepharophimosis, blepharoptosis, telecanthus, hypertelorism or hypotelorism, upslanted or downslanted palpebral fissures, epicanthus, arched eyebrows, strabismus, esotropia, microphthalmia, iris coloboma, nystagmus, anisocoria, megalocornea, iris hypoplasia, oculomotor paralysis, astigmatism, blue sclera, deep optic nerve cupping, immature retinal vessels, and tortuosity of retinal vessels.

28. Gigablast Search Results Internet Addiction@ (22); Interstitial Cystitis@ (28); Intestinal Flu@ (10);Intracranial Hypotension@ (1); intrauterine dwarfism@ (3); Iritis@ (19) http://dir.gigablast.com/Health/Conditions_and_Diseases/I/

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29. JustCan.com Disability Directory Intracranial Hypotension@ (1); intrauterine dwarfism@ (3); Iritis@ (19);Irritable Bowel Syndrome@ (60); Isaacs Syndrome@ (3); Itching@ (6) http://directory.justcan.com/odpphp/odp.php?browse=/Health/Conditions_and_Diseas

30. I Internet Addiction Interstitial Cystitis Intestinal Flu IntracranialHypotension intrauterine dwarfism Iritis Irritable Bowel Syndrome http://www.ebroadcast.com.au/dir/Health/Conditions_and_Diseases/I/

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32. Login Am J Med Genet 6210 –15 First citation in article PubMed; Russell A (1954) Asyndrome of intrauterine dwarfism recognizable at birth with craniofacial http://dx.doi.org/10.1086/302717

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33. I Health, Directory intrauterine dwarfism Impulse Control Disorders Imperforate Hymen Incontinence Isaacs Syndrome Insulin Resistance http://www.lila-ilab.org/bGlfNDMzNTE=.aspx

Health, I Top Health Conditions and Diseases I ... Interstitial Cystitis :: Directory Links :: Other Links Friday 9/9/2005 3:19 AM

34. EMedicine - Skeletal Dysplasia : Article By Harold Chen, MD, MS, FAAP, FACMG Skeletal Dysplasia dwarfism is a commonly used term for intrauterine growthretardation, such as maternal insufficiency due to drugs, ethanol, http://www.emedicine.com/ped/topic625.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Skeletal Dysplasia Last Updated: April 4, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: disproportional short stature, short stature, dwarfism, osteochondrodysplasias, thanatophoric dysplasia, achondroplasia, osteogenesis imperfecta, achondrogenesis, chondrodysplasia punctata, homozygous achondroplasia, chondrodysplasia punctata, camptomelic dysplasia, congenital lethal hypophosphatasia, perinatal lethal type of osteogenesis imperfecta, short-rib polydactyly syndromes, hypochondroplasia, rhizomelic type of chondrodysplasia punctata, Jansen-type metaphyseal dysplasia, spondyloepiphyseal dysplasia congenita, atelosteogenesis, diastrophic dysplasia, congenital short femur, Langer-type mesomelic dysplasia, Nievergelt-type mesomelic dysplasia, Robinow syndrome, Reinhardt syndrome, acrodysostosis, peripheral dysostosis, Kniest dysplasia, fibrochondrogenesis, Roberts syndrome, acromesomelic dysplasia, micromelia, Morquio syndrome, Kniest syndrome, metatrophic dysplasia, spondyloepimetaphyseal dysplasia AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Harold Chen, MD, MS, FAAP, FACMG

35. Seckel's Syndrome (www.whonamedit.com) Seckel s syndrome An intrauterine form of dwarfism. Also known as Harper’ssyndrome,Seckel s bird head syndrome,Seckel s nanism,VirchowSeckel syndrome. http://www.whonamedit.com/synd.cfm/869.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Seckel's syndrome Also known as: Harper’s syndrome Seckel's bird head syndrome Seckel's nanism Virchow-Seckel syndrome Synonyms: Bird-headed dwarfism, birdlike face syndrome, microcephalic primordial dwarfism, nanocephalic syndrome, nanocephaly syndrome. Associated persons: Rita G. Harper Helmut Paul George Seckel Rudolf Ludwig Karl Virchow Description: An intrauterine form of dwarfism characterized by proportional short stature, reduced circumference of the cranium, a characteristic bill-like protrusion of the central area of the face with microcephaly, prominent sometimes beaked nose, large ears, sparse hair, joint defects, clubfoot, trident hands, absence of some teeth, cloacalike malformation of genitourinary tract and rectum, mental retardation and sweet disposition. A small, simplified cerebrum resembles the chimpanzee brain (pongidoid microcephaly. There is a reduction in the number of blood cells. Both sexes affected; present at birth. Inheritance is autosomal recessive. There has been described a case in which all the features of the syndrome were present, but not the dwarfism. This could be an incomplete form or a variant of the syndrome.

36. Taybi-Linder Syndrome (www.whonamedit.com) A syndrome of intrauterine growth retardation characterized by dwarfism, lowbirth weight, cerebral dysgenesis, and bone dysplasia. http://www.whonamedit.com/synd.cfm/3414.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Taybi-Linder syndrome Synonyms: Cephaloskeletal dysplasia, osteodysplastic primordial dwarfism type I and III, microcephalic osteodysplastic dwarfism Type I and II, microcephalic primordial dwarfism type I and III. Associated persons: David Linder Hooshang Taybi Description: A syndrome of intrauterine growth retardation characterized by dwarfism, low birth weight, cerebral dysgenesis, and bone dysplasia. Inheritance is probably autosomal recessive. Bibliography: H. Taybi, D. Linder:

37. Dwarfism - Short Stature dwarfism and short stature information, links to national and international Transition to Adult, intrauterine Growth Retardation, Hypothyroidism, http://www.kumc.edu/gec/support/dwarfism.html

Dwarfism / Short Stature (Skeletal Dysplasias, Achondroplasia, Jeune Syndrome constitutional delay , other conditions) Organizations Clinics International Specific Syndromes ... Little People of America (LPA) , Inc. P.O. Box 745, Lubbock, TX 79408 E-mail: LPADataBase@juno.com Web Site: www.lpaonline.org Little People of America Teen Page, Books Organization Links Types of Dwarfism and Definitions LPA Parents' Forum (not currently active, web only), Mayeux family, jmayeux@gte.net LPA Parents' Committee - Rob and Betty Jacobsen, 3010 Olympia Way, Longview, WA 98632, Voice: 360.636.0276, BBS/fax: 360.578.1948, E-mail: jacobsen@aone.com Frequently Asked Questions Languages: English, Spanish dwarfism.org Billy Barty Foundation, Inc. 929 W Olive Avenue, Suite C, Burbank, CA 91506 Phone: (818) 953-5410 Fax: (818) 953-7129 Web site: www.rth.org/bbf/ Educational and lobbying for individuals with dwarfism Human Growth Foundation 7777 Leesburg Pike (P.O. Box 309), Falls Church, VA 22043 Phone: (800) 451-6434 or (703) 883-1773 Fax: (703) 883-1776 Supports basic clinical research pertaining to growth disorders. Disseminates information. Encourages development of local parent support groups. Oversees a grant research program

38. Russell-Silver Syndrome For families with children who have Russell Silver intrauterine growth dwarfism / short stature resources, University of Kansas Medical Center http://www.kumc.edu/gec/support/russell.html

Russell-Silver Syndrome Russell-Silver Syndrome Network Division of MAGIC Foundation 6645 W. North Ave. Oak Park, IL 60302 Phone: 708.383.0808 / 800-3-MAGIC-3 Fax: 708.383.0899 E-mail: mary@magicfoundation.org Web page: http://www.magicfoundation.org Association for Children with Russell-Silver Syndrome, Inc. 22 Hoyt Street Madison, NJ 07940-1604 Phone: (201) 377-4531 or (313) 242-2219 Fax: (201) 822-2715 c/o Jodi Zwain For families with children who have Russell Silver intrauterine growth retardation Also See: National organizations , resouces for genetic conditions or birth defects Dwarfism / short stature resources University of Kansas Medical Center To locate a genetic counselor or clinical geneticist in your area: Professional Genetics Societies Genetic clinics, centers, departments Revised November 8, 2002 Genetic Societies Clinical Resources Labs Clinics ... Search Genetics Education Center Debra Collins, M.S. CGC , Genetic Counselor, dcollins@kumc.edu This site subscribes to the principles of the HONcode (Health on the Net, Code of Conduct for Medical and Health Web Sites)

39. Evaluation Of Stillbirth (Intrauterine Fetal Demise) Evaluation of intrauterine Fetal Demise. on the AP film or to define bonessuspected or known to have a structural anomaly • If dwarfism is present, http://www.obfocus.com/SanGabriel/guidelines/iufd.htm

San Gabriel Valley Perinatal Medical Group HOME OUR OFFICES OUR DOCTORS SEARCH Evaluation of the Stillbirth Translate The purpose of this guideline is to help identify high risk populations and aid in the development of risk-reducing interventions. In addition it is hoped that families will be provided with information about the cause of death, as well as emotional guidance. Stillbirth may be suspected when the mother ceases to feel fetal movement, and the obstetrician is unable to hear fetal heart tones. When the question of fetal death arises during labor, an internal fetal monitor can be applied to the presenting part. Maternal cardiac electrical activity can be transmitted through a dead fetus, however, so the rate and rhythm on the tracing should be compared with those of the mother. BACKGROUND Data from the National Center for Health Statistics showed a fetal mortality rate of 6.5 per 1000 births in 2001 [1]. Risk factors associated with stillbirth [1,2-4] Maternal age (both high and low) Unmarried status Male fetal sex Multiple gestation.

40. A Novel Developmental And Immunodeficiency Syndrome Associated With Intrauterine are characterized by dwarfism (intrauterine onset) and mental retardation . The syndrome is also different from other primary forms of dwarfism http://pediatrics.aappublications.org/cgi/content/full/113/1/136

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract Full Text (PDF) P ... Citation Map Services E-mail this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Download to citation manager Search for citing articles in: ISI Web of Science (3) PubMed PubMed Citation Articles by Bernard, F. Articles by Casanova, J.-L. Related Collections Related AAP Red Book topics: Cytomegalovirus Infection PEDIATRICS Vol. 113 No. 1 January 2004, pp. 136-141 EXPERIENCE AND REASON A Novel Developmental and Immunodeficiency Syndrome Associated With Intrauterine Growth Retardation and a Lack of Natural Killer Cells ABSTRACT TOP ABSTRACT CLINICAL REPORTS DISCUSSION REFERENCES Objective. To describe a novel syndrome characterized by severe prenatal and postnatal growth failure, mild skeletal and facial abnormalities, and primary immunodeficiency. Design. The syndrome was observed in 2 sisters. The elder child died of cytomegalovirus infection when she was 18 months old

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