41. RainbowKids Waiting Children Of The World All appropriate tests have been done and all the tests have found no internal concerns. He has been diagnosed with dolicocephaly. http://www.rainbowkids.com/wc/viewChild.jsp?oid=10604

42. Program Nr 855 Patient 1 is an 18 year old severely mentally impaired male with dolicocephaly, high arched palate, flat nasal bridge, acquired total alopecia, prominent ears http://www.faseb.org/genetics/ashg00/f855.htm

Program Nr: 855 Deletion of 2q37 and duplication of 10q24: Report of two cases in the same family and literature review. A. Wiktor , G.L. Feldman , E. Bawle , P. Czarnecki , J. Conard , D.L. Van Dyke 1) Department of Medical Genetics, Henry Ford Health System, Detroit, MI; 2) Division of Genetic and Metabolic Disorders, Children's Hospital of Michigan, Detroit, MI; 3) Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI.

43. 829: Overlapping Features Of Prader-Willi Syndrome And Trisomy 18 During Infancy She had a narrow bifrontal diameter, dolicocephaly with mild ridging of the sagittal and metopic sutures, almond shaped eyes, a small mouth with a thin upper http://www.faseb.org/genetics/ashg99/f829.htm

Program Nr: 829 Overlapping features of Prader-Willi syndrome and trisomy 18 during infancy. H.A. Ishmael , L.M. Pasztor , P.G. Rothberg , J. Pfotenhauer , V. Hannig , M. Summar , M.G. Butler 1) Section of Medical Genetics and Molecular Medicine, The Children's Mercy Hospitals and Clinics, Kansas City, MO; 2) Division of Medical Genetics, Department of Pediatrics, Vanderbilt University, Nashville, TN.

44. J. Orthod. -- Taylor 30 (2): 175 forms in cephaly, where we actually have orthocephaly, the condition of being normal-headed, normal-headedness, beside brachycephaly, dolicocephaly, etc. http://jorthod.maneyjournals.org/cgi/content/full/30/2/175

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: PDF Version of this Article Email this article to a friend Similar articles found in: J. Orthod. Online PubMed PubMed Citation Search PubMed for articles by: Taylor, G. S. Alert me when: new articles cite this article Download to Citation Manager Journal of Orthodontics, Vol. 30, No. 2, 175-177, June 2003 British Orthodontic Society Features Section Orthodontics v Orthodontia G. S. Taylor Helensburgh, UK Correspondence: G. S. Taylor, 47 Millig Street, Helensburgh, G84 9PN, UK. Email: stuart@s-taylor.prestel.co.uk In this short paper I will give an account of how the dental that name. Contemporary accounts indicate that the founding fathers of consideration. was intended to emphasize that it was not the intention to form a group of specialists discussing particular systems of treatment. All people having an interest in the subject of orthodontia, dental and non-dental, would be welcome. George Northcroft was The term reflected an interest in overall facial configuration and not just limited to the relationship of dental tissues.

45. Hum. Mol. Genet. -- Price Et Al. 7 (3): 563 Several other clinical features, including macrocephaly, dolicocephaly, a high prevalence of dental caries, narrowing of the ear canal, altered craniofacial http://hmg.oupjournals.org/cgi/content/full/7/3/563

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Abstract of this Article PDF Version of this Article Email this article to a friend Similar articles found in: Hum. Mol. Genet. Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Price, J. A. Hart, T. C. Alert me when: new articles cite this article Download to Citation Manager Human Molecular Genetics Pages Identification of a mutation in associated with tricho-dento-osseous (TDO) syndrome Introduction Results Identification of a common haplotype in the TDO region Mapping of DLX7 to the common haplotype region and mutational analysis ... References Identification of a mutation in associated with tricho-dento-osseous (TDO) syndrome Jennifer A. Price Donald W. Bowden J. Tim Wright Mark J. Pettenati Thomas C. Hart Department of Biochemistry, Department of Pediatrics, and Department of Dentistry, Wake Forest University School of Medicine, Bowman Gray Campus, Winston-Salem , NC 27157, USA and Department of Pedodontics, University of North Carolina School of Dentistry

46. BJU International (February 1999), 83.3 mental retardation, advanced bone age, and facial dysmorphic features including frontal bossing, antimongoloid slant, palpebral fissures and dolicocephaly (Fig http://www.bjui.org/83/3/article/bju988.asp

Quick Search: You are in: Home Online Content List of Issues BJU International (February 1999), 83.3 Testicular yolk sac tumour in a patient with Sotos syndrome O Muraishi , T Kumamaru , Y Nozaki , Y Mori and A Tokue Departments of Urology, Pediatrics, Jichi Medical School, Tochigi, Japan Case report Comment References Fig. 1 ). The patient was followed up without further adjuvant therapy. Serum AFP levels decreased gradually and became almost normal (8 ng/mL) at 7 months after surgery. The overgrowth disorder of the patient was followed in the paediatric department. His weight and length were 15.4 kg and 90 cm at the age of 14 months. The patient was diagnosed as having Sotos syndrome by his clinical characteristics, i.e. excessive growth during the first year of life, mental retardation, advanced bone age, and facial dysmorphic features including frontal bossing, antimongoloid slant, palpebral fissures and dolicocephaly ( Fig. 2 Comment Case report References Sotos syndrome is characterized by accelerated growth, minor craniofacial anomalies and intellectual deficits. An increased incidence of malignancies among Sotos syndrome patients has been suggested [ ]. A review of the world literature revealed no reported case of testicular tumour in Sotos syndrome. This patient developed yolk sac tumour in the left testis at 6 months and was diagnosed as having Sotos syndrome after 9 months of follow-up in the paediatric department. This is the first reported case of testicular yolk sac tumour occurring with Sotos syndrome.

47. Genes At Work - Topics In Genetics dolicocephaly is a common finding as are downslanting palpebrae, a prominent jaw, a high arched palate, facial flushing, premature dental eruption, large http://www.umdnj.edu/genesatwork/topics/pediatrics/11_pediatrics.htm

Overgrowth Syndromes: an Overview by Beth A. Pletcher, MD, May 1999 Even though the majority of individuals with BWS represent new mutations or genetic event in the family, there are a number of reports of autosomal dominant transmission of this disorder. Because chromosomal duplications, cytogenetic translocations as well as monozygotic twins discordant for BWS have all been seen, it is clear that this is genetically heterogeneous and can occur post-zygotically resulting in somatic mosaicism (some cells with the BWS mutation and some without). In fully 10-20% of patients with BWS, molecular studies demonstrate paternal uniparental disomy (UPD) which suggests that there are two paternal #11 chromosomes and no maternal contribution. In all of these cases identified thus far mosaicism has been seen which suggests a post-zygotic error during cell division. Point mutations in three genes so far have been shown to cause BWS. First, mutations in p57kip2, a cyclin dependent kinase inhibitor, have been seen in: sporadic cases, many maternally transmitted BWS and a much smaller percentage of paternally transmitted BWS. This gene in particular has a high association with omphalocele and cleft palate.

48. Abstract of having Sotos syndrome due to polyhydramnios in her motherís pregnancy, large birth weight and length, macrocephaly, dolicocephaly, frontal bossing http://www.biologia.uniba.it/fecc/7_39.htm

ABSTRACT Clinical Sotos syndrome with del(5)(qter) detected by subtelomeric FISH analysis. J. M. D. Hahnemann , B. Kassow , K. Nielsen , L. Buchardt , P. Baekgaard and M. Dunoe Medical Genetics Laboratory Center, The John F. Kennedy Institute, Glostrup, Denmark Center of Childrenís Neurology, Dept. Paediatrics, Glostrup University Hospital, Glostrup, Denmark Molecular Genetics Laboratory, Dept. Clinical Genetics, Rigshospitalet, Copenhagen, Denmark ponsible for this syndrome, NSD1, is located in 5q35. A real-time quantitative PCR approach subsequently confirmed that the deletion included exon 5 of the NSD1 gene. This is to our knowledge the first diagnosis of Sotos syndrome through subtelomeric FISH. Deletions of the whole NSD1 gene were originally reported by a Japanese group to be the most frequent type of mutation among persons with Sotos syndrome. Mapping of the size of the deletion by FISH is in progress. Authors Home Page Keywords Abstracts will be published by Elsevier (Annales de GÈnÈtique)

49. Entrez PubMed advanced growth. Minor anomalies include dolicocephaly, abnormal ears, ptosis, dysplastic toenails, and relatively large hands. As http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

50. Entrez PubMed appearance of the two cases we have observed was that of mental retardation and typical features including abnormal facies (dolicocephaly, frontal prominence http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstra

51. Blackwell Synergy - Cookie Absent overgrowth, advanced bone age, psychomotor and mental delay and muscle weakness (5,7,8). Other findings include dolicocephaly, prognathism, hypertelorism, high http://www.blackwell-synergy.com/links/doi/10.1046/j.1460-9592.2003.01158.x/abs/

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

52. Blackwell Synergy - Cookie Absent On physical examination, he showed mild dysmorphic features consisting of dolicocephaly, high arched palate, hypoplasia of the scapha helix, synophris http://www.blackwell-synergy.com/links/doi/10.1034/j.1399-0004.2000.570514.x/abs

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

53. Is Three-dimensional Ultrasound Adding New For Detection Of Congenital Anomalies 2. Trisomy 21; hydramnios. 26,28. 2. Microcephaly. 26,36. 1. dolicocephaly. 34. 3. Anencephaly; hydramnios. 2932. 2. Occipital encephalocele (twin). 24,26. 1. http://www.gfmer.ch/International_activities_En/El_Mowafi/Three-dimensional_ultr

Diaa M. El-Mowafi - Zagagig University, Egypt Is three-dimensional ultrasound adding new for detection of congenital anomalies? Diaa M. El-Mowafi MD Associate Professor, Department of Obstetrics and Gynecology, Benha Faculty of Medicine, Egypt Fellow, Geneva University, Switzerland Abstract Objective: to evaluate the three-dimensional ultrasound (3D US) as a recent method for detection of fetal congenital anomalies in comparison with the traditional 2 D US. Materials and Methods: Thirty-eight fetuses had been examined with the same equipment containing the traditional 2D US and 3D US. Each fetus had been scanned with one volume probe that has the 2 options; 2D and 3D US. The gestational ages of the examined fetuses were 22-36 weeks. Results: Seventy-two abnormalities were detected with 2D US, real-time 3D US, or both in 38 fetuses. Of the 72 fetal abnormalities, sixteen (22%) that had not been identified adequately at 2D US were disclosed with real-time 3D US. For eighteen abnormalities (25%) diagnosed at 2D US, real-time 3D US gave further information. Thirty-eight abnormalities (53%) were diagnosed only with 2D US. Conclusion: Real-time 3D US is useful for evaluating fetal abnormalities as a supplement to 2D US, particularly for abnormalities of the face, head, fingers, and skeleton, but real-time 3D US is unlikely to be helpful for detecting intra-fetal abnormalities except for skeletal abnormalities and some pathologic changes with fluid accumulation.

54. ADC -- Clayton 78 (2): 185 The dysmorphic features which have been described include microcephaly, dolicocephaly, a large fontanelle, a triangular facies with down slanted eyes and long http://adc.bmjjournals.com/cgi/content/full/archdischild;78/2/185

HOME HELP FEEDBACK SUBSCRIPTIONS ... Email this link to a friend eLetters: Submit a response to this article Similar articles in ADC Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Clayton, P. T Alert me when: new articles cite this article Download to Citation Manager Arch Dis Child 185-189 ( February ) Current topic Disorders of cholesterol biosynthesis Peter T Clayton Biochemistry Unit, Institute of Child Health and Metabolic Unit, Great Ormond Street Hospital for Children, London Correspondence to: Dr Peter T Clayton, Biochemistry Unit, Institute of Child Health, 30 Guilford Street, London WC1N 1EH. Functions of cholesterol Top Functions of cholesterol Sources of cholesterol Biosynthesis of cholesterol Disorders affecting the... Disorders affecting the... Drugs which inhibit the... Treatment of SLO syndrome... References Sterols are important constituents of the cell membranes of most eukaryotic cells. The cell membranes of terrestrial vertebrates, including man, contain a single major sterol species

55. Sci.anthropology.paleo: Re: Homo Heidelbergensis Partial albinism, vestigal brow ridges (I can feel mine distinctly), second toes longer than first toes (well, mine are), relative dolicocephaly (at least http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive

Re: Homo heidelbergensis Michael Siemon ( mls@panix.com 30 May 1994 20:11:13 -0400 Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Previous message: Stanley Friesen: "Re: Homo heidelbergensis" Umm, this turns out not to be the case :-) There is indeed a fair amount of genetic assimilation from neighboring populations, but not enough to overbalance the similarities of geographically separated populations of Jews. Some substantial references to (recent) work on this were posted when the matter received an intensive net airing some 6 months to a year ago. I didn't save the references, but those who posted them were names I hold in some considerable respect. I expect your assertion will give rise to your receiving citations that should satisfy your scrutiny. The one point I'd suggest against Stan's note is his 2500 year figure I'd put it at more like 1000-1500 years the Mediterannean Jewish community was not at all separated into distinct populations in Roman times or for some while thereafter. Even the Muslim conquests will not have been more than an easily permeable barrier. European Jewry became quite isolated

56. Sci.anthropology.paleo: Re: Homo Heidelbergensis ridges (I can feel mine distinctly), second toes longer than first toes (well, mine are), relative dolicocephaly (at ^^^^^ least http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive

Re: Homo heidelbergensis Xiaoguang Zhang ( zhang@gmsds.ms.ornl.gov Sun, 5 Jun 1994 21:01:30 GMT Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Next message: Cameron Laird: "Re: aquatic ape?" Previous message: Stanley Friesen: "Re: Early diets" Maybe in reply to: NICHOLLS PHILIP A: "Homo heidelbergensis" Ken Brown (rkjb@cix.compulink.co.uk) wrote: : Back on topic for a while - I have a purely sentimental attraction to the : idea that some of the oddities about us northern Europeans are due to : Partial albinism, vestigal brow ridges (I can feel mine distinctly), second : toes longer than first toes (well, mine are), relative dolicocephaly (at : least amongst early populations, it seems to have diminished in the last : millenium)... until someone proves the contrary with genetic evidence I shall : persist in imagining that I have a few Neanderthal ancestors! I wonder if this constitutes counter argument: I'm a Chinese, and my second toes are longer than first toes. Same for my wife (also a Chinese). Does that mean that I too have a few Neanderthal ancestors?

57. Science - Ethics - Power, Turner Statement Regarding Eugenics of the small sample size they had managed to collect, no statistically significant correlations could be established between dolicocephaly and mesocephaly or http://www.umich.edu/~idpah/SEP/sep_te.html

EUGENIC IDEAS IN JAMES NEEL'S CONCEPTION OF "PRIMITIVE SOCIETY" Terence Turner Department of Anthropology, Cornell University November 10, 2000 A puzzling feature of the outpouring of messages and testimonials in support of James Neel against the allegations about his actions and ideas in Patrick Tierney's book, Darkness in El Dorado, is the denial that Neel held eugenic beliefs. In his discussions of primitive society, Neel was quite explicit about his eugenic ideas, both in print and in conversation. They have a fundamental place in his conception of the selective advantages of primitive (and specifically Yanomama) social organization. These ideas are most fully expounded in his article, "On being Headman". I quote at length from this article. I have put certain passages in upper case for emphasis (page numbers are indicated in brackets). [p.285-] Some genetic implications of [Yanomami] culture Some caveats Are there tenable countermeasures to the loss of our primitive population structure? Menu of Resources Doctoral Program in Anthropology and History

58. Deflexion - ThesaurusDictionary.com :: All About Deflexion Hypertonicity of the extensor muscles of the neck. dolicocephaly long anteroposterior diameter of the head, so as the breadth is less than 4/5 of the length. http://www.thesaurus-dictionary.com/files/d/e/f/deflexion.html

Search for a new word: a b c d ... z Previous Word: deflexed deflexure wainage Focus Word: deflexion 1. see deflection. Thesaurus Terms for: deflexion bending bend movement motion ... Free Everything The Best Sites for: deflexion Face Presentation - D. El-Mowafi Hypertonicity of the extensor muscles of the neck. Dolicocephaly: long antero-posterior diameter of the head, so as the breadth is less than 4/5 of the length. Pendulous abdomen or marked lateral obliquity of the uterus. Further deflexion of brow... i-...... http://matweb.hcuge.ch/El_Mowafi/face_presentation.htm Curvature Roget's Thesaurus: Entry 245 (Curvature)245. Curvature. N. curvature, curvity[obs], http://www.astro.caltech.edu/~pls/roget/entries/245.html Glossary Glossary Note : This is not intended to cover all the words used about bridges. Some words have been included that have not been mentioned earlier, as they are of general interest; and in some cases a fuller explanation or comment is supplied. Arches... http://www.media.uwe.ac.uk/masoud/projects/bridges/text/glossary/glossary.htm Rutherford's Followup to his 1911 Paper 488 The present paper and the accompanying paper by Mr. C. Darwin deal with certain points in

59. 107 dolicocephaly. References 2,index, home, previous. http://www.zdmu.ac.ir/nnd/nd0399/1998/10/107.htm

Dolicocephaly References index home previous

60. OB-GYN-L Messages For December, 2002: Re: OB U/S--Significance Of Cephalic Index 7483%). dolicocephaly, You re familiar with, results from AP elongation as occurs with breech (maternal rib cage) or oligo. The http://fercenter.com/forums/obgynl/obgynl.0212/0179.asp

Login Home Register Search ... Contact The OB-GYN-L discussion forum is provided for the use of Ferring by OBGYN.net. Ferring provides this resource to its readers for their convenience but does not review or control the discussion list nor any of its contents. Therefore, the information provided in this discussion forum does not constitute any endorsement by Ferring for any purpose or use. Re: OB U/SSignificance of Cephalic Index From: Terrence.Jones@kp.org Sun Dec 15 17:24:24 2002 Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Next message: Braun, R. Daniel: "Re: OB U/SSignificance of Cephalic Index" Previous message: Len2976@aol.com: "OB U/SSignificance of Cephalic Index" Maybe in reply to: Len2976@aol.com: "OB U/SSignificance of Cephalic Index" Next in thread: Dr. John Provatopoulos B.Sc. M.D.C.M. F.R.S.C.: "Re: OB U/SSignificance of Cephalic Index" Reply: Dr. John Provatopoulos B.Sc. M.D.C.M. F.R.S.C.: "Re: OB U/SSignificance of Cephalic Index" This is a multipart message in MIME format. =_alternative 0000E0C388256C91 Content-Type: text/plain; charset="us-ascii" Len2976@aol.com

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