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
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
Extractions: 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.
Extractions: 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.
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
Extractions: British Orthodontic Society 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.
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
Extractions: References 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
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
Extractions: 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.
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
Extractions: 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.
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
Extractions: 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)
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
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
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/
Extractions: 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.
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
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Extractions: 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.
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
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
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
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
Extractions: 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
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
Extractions: 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. From: Terrence.Jones@kp.org
