An American-Swedish Dialogue On Racial Issues instead of Nordic as the inclusive term for all Northern Europeans, as Ripley and others defined Nordics by certain physical traits (dolicocephaly, light hair http://www.racialcompact.com/Swedish_email.html
Extractions: To: archon@racialcompact.com Greetings sir, What you wrote on "The Racial Compact" and other material is not only the most intelligent I have read about racial issues, but it's outstandingly similar to what I realized myself. After surfing on the net for years I was resigned to find just rednecks and hooligans in bombers and "Doc Marten's". I came too to the concept of "The Racial Golden Rule", and, oddly enough, I came also to think to the Prime Directive of Star Trek (I'm a science fiction fan too, even if I ceased to look Star Trek when I realized it's a subtle propaganda of the American melting pot). Is it all hopeless? I don't think so, and if it doesn't bother you, I would discuss the issue with you further. My most respectful greetings. P.E. Dear P.E.
ESHG Posters 3 The variability of clinical manifestations included dolicocephaly with or without sagittal suture synotosis, sparse hair, thin nails, brachydactyly, and http://www.medacad.org/eshg/abstracts/posters3.htm
Extractions: Department of Medical Genetics, Rabin Medical Center, Petah Tiqva, ISRAEL, Pediatric Intensive Care Unit, Dana Children's Hospital, Tel Aviv Medical Center,, Tel Aviv, ISRAEL, Division of Pediatric Intensive Care Unit, Schneider Children's Medical Center,, Petah Tiqva, ISRAEL, Department of Neonatology, Rabin Medical Center, Petah Tiqva, ISRAEL. Solitary median maxillary central incisor (SMMCI) has been reported as an isolated abnormality or in association with other systemic abnormalities including pituitary insufficiency, nasal pyriform aperture stenosis and holoprosencephaly. SMMCI can also be a feature of recognized syndromes or chromosomal abnormalities. SHH and SIX3 mutations have been reported in patients with SMMCI. We report on an infant with a previously undescribed pattern of malformations including brachycephaly, proptosis, midfacial hypoplasia, SMMCI, abnormal ears, arachnodactyly, partial cutaneous syndactyly and joint contractures. CT scan revealed pyriform aperture stenosis. At the age of eleven months, the patient has developmental delay and suffers from seizures. Laboratory investigations were within normal limits. Roentgenologic skeletal survey was normal apart from the finding of 11 pairs of ribs. CT scan of the brain was normal. BAER examination revealed hearing loss on the left side. Chromosomal studies including high-resolution chromosomal analysis showed a normal female karyotype. Sequencing of the exons IIIa and IIIc of FGFR2 did not reveal mutations.
Special Child: Diagnosis Search premature closure); dolicocephaly (long, narrow head); Slight epicanthal folds (vertical fold on either side of the nose); Lowset http://www.specialchild.com/diagnosis013.html
Extractions: Diagnosis Search The parents of this child are anxiously searching for a diagnosis. If you have any information or suggestions you would like to share with them, please send an e-mail to DiagnosisSearch@specialchild.com . Please be sure to mention the name of the child you are referring to so that your message can be immediately forwarded to the parent. Thank you for taking the time to stop by - we appreciate your interest in helping parents with their search. Hayley Kabana, DOB 4/8/94 Features and Characteristics: Hydrocephalus (with VP shunt) Seizures Mild bilateral hearing loss Hypotonia Ligamentous laxity (wears SMOs but can ambulate well) Atrial septal heart defect (repaired) Mental retardation (mild to moderate) Strabismus and sensitive to sunlight Chronic elevated liver enzymes Ketotic hypoglycemia Beau's lines (ridges in the fingernails) Constipation Stridor (a harsh vibratory sound caused by an upper airway obstruction) at night Difficulty maintaining body temperature Mild frontal bossing (prominent forehead) Macrocephaly Flat supraorbital ridges (above the eye cavity) Widely-spaced eyes Downward turned palpebral fissures (opening between the eyelids) Widely-spaced teeth Prominent scaphocephaly (abnormal length and narrowness of the skull as a result of premature closure) Dolicocephaly (long, narrow head)
The New Health Directory Identity Disorder@ (106); Diverticulitis@ (24); dolicocephaly@ (0); Down Syndrome@ (88); Drooling@ (2); Dry Eye@ (4); Duane Retraction http://www.thenewhealthfind.com/Health/ConditionsandDiseases/D/
Sagittal Synostosis Also known as scaphocephaly or dolicocephaly, the sagittal suture closes early and restricts groth of the head in the side to side direction. http://cpmcnet.columbia.edu/dept/nsg/PNS/cf/sagittal.html
Extractions: Also known as scaphocephaly or dolicocephaly , the sagittal suture closes early and restricts groth of the head in the side to side direction. This forces the head to grow in a front to back direction which leads to a narrow elongated head. Usually there is an associated fullness or "bossing" to the forehead.
4Reference || Audin/experiment dolicocephaly, flattened coronal suture, narrowed intraorbital distance, elbow dysplasia, shortened ulna, pseudoepiphyses of the second metacarpal bone http://www.4reference.net/encyclopedias/wikipedia/Audin_experiment.html
Extractions: Front Page Encyclopedias Dictionaries Almanacs ... Quotes Audin/experiment NOTOC Funded by the NIH * Developed at the University of Washington, Seattle [3M Dwarfism] Authors: Muriel Holder-Espinasse, MD Robin M Winter, FRCP, F Med Sci About the Authors Initial Posting: 25 March 2002 Last Revision: 8 May 2002 - =Summary= Disease characteristics. 3-M syndrome is characterized by pre- and postnatal growth retardation, distinctive dsflkgjd facial features (relatively large head, frontal bossing, triangular face, pointed djhgls and prominent chin, fleshy and upturned nose, full lips, full eyebrows, and a hypoplastic midface), and radiological abnormalities. Intelligence is normal. Diagnosis/testing. The diagnosis of 3-M syndrome is suggested in children with a low birth weight, severe growth retardation, a final height between 5 and 6 SD below the mean, and characteristic facies. Characteristic radiological findings are slender long bones, thin ribs, foreshortened vertebral bodies appearing tall, spina bifida occulta, small pelvis, small iliac wings, and retarded bone age. There are no diagnostic laboratory findings, and the molecular basis of the syndrome is still unknown. Genetic counseling.
3802cr5 bridge and long trunk(4). More recently in 1992, Phelan et al reported a threeyear-old with developmental delay, hypotonia, dolicocephaly, ptosis, epicanthal 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.
Program Nr 95 dysmorphic features include dysplastic toenails, relatively large fleshy hands, prominent and/or dysplastic ears, pointed chin, dolicocephaly, ptosis, and http://genetics.faseb.org/genetics/ashg01/f95.htm
Deskmod.org Health Conditions And Diseases D Top / Health / Conditions_and_Diseases / D See also dolicocephaly, Diabetes, Dystonia Musculorum Deformans, Depersonalization Disorder, Diabetic Retinopathy. http://www.deskmod.org/Health/Conditions_and_Diseases/D
CHROMOSOMAL DUPLICATION/DEFICIENCY SYNDROMES The most commonly observed deletions in humans are 4p (Wolf-Hirschhorn syndrome microcephaly, dolicocephaly, hipoplasia of the eye socket, ptosis, strabismus http://malattierare.pediatria.unipd.it/pubblicaMR/mr_dx_ing.asp?mr=343
Table 1 170 degreesProtrusio acetabulae (radiographs)Pes planus due to medial displacement of medial malleolus, Characteristic facies (dolicocephaly, malar hypoplasia http://www.biomedcentral.com/1537-890x/id/cr-sr1211/table/T1
Extractions: Arm span-to-height 1.05Lower body height to upper body height 1.05Chest wall abnormalities (severe pectus excavatum)Spine abnormalities (scoliosis 20 degrees or spondylolisthesis)Positive wrist and thumb signsElbow extension 170 degreesProtrusio acetabulae (radiographs)Pes planus due to medial displacement of medial malleolus
Www.paediatrics.ws Otherwise unusual head shapes were noticed in 3 multiplebirth infants, including cephalohematoma, dolicocephaly, and frontal bossing (n = 1). http://www.paediatrics.ws/html/clinical_journals/j5.htm
Top / Health / Conditions_and_Diseases / D Top / Health / Conditions_and_Diseases / D See also dolicocephaly, Diabetes, Dystonia Musculorum Deformans, Depersonalization Disorder, Diabetic Retinopathy. http://www.checkburst.com/Health/Conditions_and_Diseases/D
