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Journal Of Pediatric Hematology Oncology - UserLogin After the skin edema subsided, he was noted to have facial features consistentwith NS, as evidenced by dolicocephaly, downward obliquity of the palpebral http://www.jpho-online.com/pt/re/jpho/fulltext.00043426-199911000-00015.htm
The Nordish Portal Quote As for Normandy and dolicocephaly, it is not all as rare as you mightthink. If I can dig up the approximation I will post them. http://www.nordish.net/forum/showthread.php?t=1119&page=2
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
3802cr5 More recently in 1992, Phelan et al reported a threeyear-old with developmentaldelay, hypotonia, dolicocephaly, ptosis, epicanthal folds and posteriorly http://www.sma.org.sg/smj/3802/articles/3802cr5.htm
Extractions: This report describes a 5-year 6-month-old Chinese girl with partial monosomy for the long arm of chromosome 22. The karyotype was 46,XX / 46,XX,del (22) (ql3.2). She presented with global developmental delay. Clinical features include seizures, failure-to-thrive, prominent ears, long philtrum and abnormal skin pigmentation on the face and limbs. Mental retardation in association with physical abnormalities is highly suggestive of chromosomal aberrations. With the availability of increasingly sophisticated techniques in the field of cytogenetics, more patients with so-called idiopathic mental retardation and minor dysmorphic facial features may in reality have an abnormal chromosome karyotype previously undetected. Therefore, mental retardation attributed to chromosomal abnormality will be better defined with increasing awareness and reporting. CASE REPORT Psychological assessment at age 2 years 11 months confirmed global developmental delay with a functional age of approximately 15 months (Bayleys Scale of Infant development). Subsequent assessment at age 4 years 1 month showed her functioning profile to be about 17 months and speech and language skills at about 12 months.
Sci.anthropology.paleo: Re: Homo Heidelbergensis toes longer than first toes (well, mine are), relative dolicocephaly (at leastamongst early populations, it seems to have diminished in the last http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive
Sci.anthropology.paleo: Re: Homo Heidelbergensis toes longer than first toes (well, mine are), relativedolicocephaly (at ^^^^^^^^^^^^^^^^^^^^^^^^^^^^ least amongst early populations,it seems to have http://www.anatomy.usyd.edu.au/danny/anthropology/sci.anthropology.paleo/archive
The World Diseases A 2 Z Names By Countrylinks And Dr Impex dolicocephaly. Down Syndrome. Drooling. Dry Eye. Dubowitz Syndrome. Dwarfism.Dysencephalia Splanchnocystica. Dysmenorrhea. Dyspareunia. Dysphagia http://www.countrylinks.biz/diseases.htm
Phelan-McDermidin Oireyhtymä - Kehitysvammahuollon Tietopankki Kasvonpiirteisiin kuuluu pitkäpäisyys (dolicocephaly), täyteläiset kulmakarvat,silmien paksut riippuluomet, pitkät silmäripset, leveä nenänsilta, http://www.saunalahti.fi/kup/syndroma/phelan_mcdermid.htm
Extractions: Deleetio 22q13-syndrooma Mary C. Phelan kirjoitti Orphanet -artikkelissaan (2003), että oireyhtymää luonnehtii vastasyntyneen velttous, kokonaisvaltainen kehityksen viivästyminen, normaali tai kiihtynyt kasvu, puuttuva tai vaikeasti viivästynyt puhe ja pienet epämuodostumat. Kasvonpiirteisiin kuuluu pitkäpäisyys ( dolicocephaly ), täyteläiset kulmakarvat, silmien paksut riippuluomet, pitkät silmäripset, leveä nenänsilta, litteät keskikasvot, täyteläiset posket, sipulimainen nenä, suuret tai epätavalliset korvat ja kärjekäs leuka. Muita piirteitä olivat olleet suuret kädet, vajaakasvuiset varpaankynnet, puutteellinen hieneritys ja ristiluun kuoppa ( sacral dimple ). Käyttäytymistä kuvattiin autistiseksi , mihin liittyi korkea kipukynnys ja piintynyt pureskelu tai tyhjä puhe. Kromosomin 22 pitkän varren loppupäästä (geenikarttamerkintä 22q13.3) puuttui perimäainesta. Deleetio oli osoittautunut niin pieneksi, että sitä oli vaikea havaita rutiininomaisissa kromosomitutkimuksissa. Yli 30%:lle vammautuneista oli pitänyt kahdesti tai useammin kromosomitutkimus ennen kuin poikkeavuus oli löytynyt. Phelan piti oireyhtymää alidiagnosoituna, koska sitä oli niin vaikea todentaa. Oireyhtymän piirteet olivat vaikuttaneet syntymähetkellä lieviltä. Suurella osalla
What Is Phelan-McDermid Syndrome? Facial features are fairly subtle and may not be recognized by your doctor longhead shape (dolicocephaly), puffiness around the eyes, long eyelashes, http://www.22q13.org/tell_me_more/2tmm_what_is_22q13.html
Extractions: There is a wide range of severity of symptoms observed in people with the deletion, but most exhibit moderate to severe developmental delays, physically and intellectually, but especially in speaking and communicating. Very low muscle tone is a common trait of the syndrome, and many have problems with eating, sleeping and emotional stability. There are nearly 200 diagnosed cases of this deletion worldwide, but the large majority of these are small children due to the recent (1998) development of a reliable test for the deletion, so the actual number of people with the deletion is certainly much larger. Outreach to find and help these families with older children is one of the objectives of the support group.
Extractions: chromosome facts testing for 22q13 ... medical glossary There is not as much specific data on the behavior aspects of individuals with deletion 22q13 as there is in other areas. Many of the behaviors listed below were brought up in parent sharing sessions. One parent would explain a particular behavior and many others would say they have observed it with their child too. Due to this there is only one behavior with a known percentage showing what portion of the deletion population exhibit it. Some of these behaviors can be regarded as possible adaptations to physical abnormalities these individuals face. Many children with this deletion have vision issues causing them to rely on their peripheral vision. This would in turn translate to not looking people in the eye, when in reality they might be looking at people using their peripheral vision because that is the easiest way for them to see.
Extractions: Vol Page [Advanced] This Article Extract Full Text (PDF) Submit a response ... Citation Map Services Email this link to a friend Similar articles in ADC Online Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Clayton, P. T Arch Dis Child 185-189 ( February ) Peter T Clayton Biochemistry Unit, Institute of Child Health and Metabolic Unit, Great Ormond Street Hospital for Children, London
Dysostosis Multiplex Congenita - General Practice Notebook dolicocephaly; spatulate ribs oar-like; wide diaphyses and narrow epiphyses;wide metacarpals, phlanges, metatarsals - bullet-like; hypoplastic acetabulae http://www.gpnotebook.co.uk/cache/-831848417.htm
Clinical Dysmorphology - UserLogin Other less common features include dolicocephaly, dysplastic ears, pointed chin,ptosis, epicanthic folds, saddle nose, fleshy hands, dysplastic toenails, http://www.clindysmorphol.com/pt/re/mcd/fulltext.00019605-200407000-00014.htm
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.
Centronuclear And Myotubular Myopathy Information Point Patients often have typical myopathic facies with dolicocephaly, a high forehead,long face with midface hypoplasia and a narrow higharched palate with http://tonilouise.tripod.com/cnmgailreport2003.html
Extractions: Since 17th August 2003 Spotted An Error I've Missed? Please drop me a quick email so that I can correct the error and improve the site for others - Thank you TEXT size too BIG or too small for your computer? Click on View , click on Text Size and adjust accordingly Centronuclear / Myotubular Myopathy
PEDIATRICS scaphocephaly=dolicocephaly premature closure of the sagital suture. brachicoronal. trigonal metopic. occicephaly lambdoid http://radiologynotes.servehttp.com/peds/pediatrics.htm
