Extractions: Anzeige: Verdienen Sie Geld mit Ihren ungenutzten Domains! Welt English Health ... Conditions and Diseases : D A B C D E F G H ... Eintrag in weiteren Suchmaschinen Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor In einigen Teilen modifizierte Version des DMOZ.
Neurological Examination Of Newborns And Infants Much attention should be paid to the head shape dolicocephaly, brachiocephaly,towerlike skull, left or right inclination are all variants of normal skull. http://www.russianadoption.org/Neurologicalexaminationnewbornsandinfants.htm
Extractions: Meningeal signs It should be noted that neurological status of the newborns has some special features. The mainstay of investigation is the analysis of congenital reflexes which reflect the maturity if CNS, viability of the newborn and adaptation potential. The following conditions should be fulfilled during examination: comfortable room T (25-26), and it is not recommended to examine the child immediately postprandial or before feeding because feeding determinant can change the level of his congenital reflexes. It should be noted that congenital reflexes of newborns are very labile and are easily fatigued. One should elicit reflexes quickly and turn the child only after cranial and facial skeleton and cranial nerves have been already tested. It is important to look for dysembryological stigmata, which can be frequently encountered: abnormal earlobes (low amount of helixes, absence of earlobes, elongated upper part rabbit's ear, low set ears), wide nose bridge (hypertelorism), prognatism, low hair border.
Special Child: Diagnosis Search premature closure); dolicocephaly (long, narrow head); Slight epicanthalfolds (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)
Sotos' Syndrome (www.whonamedit.com) Other principal features are dolicocephaly, macrocrania, hypertelorism, antimongoloidpalpebral slant, higharched palate, frontal bossing, mandibular http://www.whonamedit.com/synd.cfm/2464.html
Extractions: Cerebral gigantism, cerebral gigantism in childhood, constitutional gigantism, gigantismus cerebralis, gigantismus constitutionalis, gigantismus idiopathicus, hypothalamic gigantism, macrostomia-mental retardation syndrome, mental retardation-overgrowth sequence, pituitary gigantism, prenatal gigantism with macrocephaly. A syndrome of excessive growth during the first 4 to 5 years of life, with cerebral gigantism and generalised large muscles in childhood, acromegalic features, and a nonprogressive cerebral disorder with nonprogressive mild mental retardation and defective coordination. After early childhood growth seems to approach normal, remaining, however, two standard deviations above means for chronological age. Birth weight and length greater than normal. Other principal features are dolicocephaly, macrocrania, hypertelorism, antimongoloid palpebral slant, high-arched palate, frontal bossing, mandibular prognathism, and precocious dentition. Occasionally, obesity, convulsions, abnormal dermatoglyphic pattern. Both sexes. Most cases are sporadic but some are transmitted as an autosomal dominant trait.
Extractions: A rare familial dysmorphy syndrome characterised by microcephaly and dolicocephaly with narrow face,, unusual facies, short stature, chest deformity, mental deficiency, and other dysmorphic features. Eye features include strabismus, short palpebral fissures, hyperopia, and hypoplasia of the optic nerve. Inheritance is X-linked.
1Up Health > Health Links Directory > Conditions And Diseases: D Syndrome (5) Digestive Disorders (785) Dimitri Disease (4) Diptheria (6) DissociativeIdentity Disorder (113) Diverticulitis (26) dolicocephaly (3) Down http://www.1uphealth.com/links/conditions-and-diseases-d.html
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Department Of Human Genetics - Clinical Features/Prader-Willi Syndrome _, Characteristic facies with dolicocephaly in infancy, narrow face or bifrontaldiameter, almond shaped eyes , small appearing mouth with thin upper lip http://www.genes.uchicago.edu/ucgs/special-diagnostics/PW-AS/PWfeatures.html
Extractions: The following is a list of clinical features associated with PWS. This list can also be used as a score sheet for patients suspected to have PWS. Score appropriately, and indicate the total score in the last box. For patients 3 years of age or younger with a score of 5 points, including at least 4 points from the MAJOR Criteria category, the PWS is likely; M-PCR is recommended. M-PCR is also recommended for patients over the age of 3 with a score of 8, with at least 5 points from the MAJOR criteria category. MAJOR Criteria (score 1 point each) Neonatal and infantile central hypotonia with poor suck, gradually improving with age. Feeding problems in infancy with need for special feeding techniques (gavage, premie nipple) and poor weight gain or failure to thrive. Excessive or rapid weight gain on weight for length chart (crossing two percentile channels) after age 12 months but before age 6 years, in the absence of intervention. Characteristic facies with dolicocephaly in infancy, narrow face or bifrontal diameter, "almond shaped eyes", small appearing mouth with thin upper lip, and/or down turned corners of the mouth. (3 or more)
AnsMe Directory - Health > Conditions And Diseases > D Dimitri Disease. Diptheria. Dissociative Identity Disorder. Diverticulitis.dolicocephaly. Down Syndrome. Drooling. Dry Eye. Duane Retraction Syndrome. http://dir.ansme.com/health/43346.html
Dolicocephaly Similar pages Craniosynostosis For families in Eastern Idaho and parts of Utah. SUBCATEGORIES. Updolicocephaly. America Medica, Inc. ®. info@medlina.com. New York. http://www.medlina.com/dolicocephaly.htm
Support Groups Sagittal Synostosis Sagittal Synostosis Homepage Sagittal synostosis (also known as scaphocephaly,dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), is a http://www.ability.org.uk/support_groups_sagittal_synostos.html
Extractions: "see the ability, not the disability" You to can help support the Ability Project by: Our Aims ... Z Support Groups Sagittal Synostosis Sagittal Synostosis Homepage - Sagittal synostosis (also known as scaphocephaly, dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), is a condition in infants where the sagittal suture (the soft spot or fontanelle on top of the head between the left and right sides of the skull) closes early and restricts growth of the head in the side to side direction. This forces the head to grow in a front to back direction, leading to a narrow elongated head. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Webmaster . Site Design by Ability "see the ability, not the disability" Acknowledgments
3802cr5 bridge and long trunk(4). More recently in 1992, Phelan et al reported a threeyear-oldwith 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.
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.
Untitled dysmorphic features include dysplastic toenails, relatively large fleshy hands,prominent and/or dysplastic ears, pointed chin, dolicocephaly, ptosis, and http://www.faseb.org/genetics/ashg01/f95.htm
A Guide To Pathology - Medical Books By Dr K Chaudhry, New Delhi includes (i) A tendency to great height (ii) Long and thin hands and feet (iii)Spinal curvatures ; Qv) Funnel or pigeon chest (v) dolicocephaly and bossing http://medicalbooks.rushsale.net/pathology/chapter14.php
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
