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         Coffin Lowry Syndrome:     more detail
  1. The Official Parent's Sourcebook on Coffin-lowry Syndrome: A Directory for the Internet Age by Icon Health Publications, 2005-01-30
  2. Coffin-Lowry Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-20
  3. Coffin-Lowry syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Roger, MD Stevenson, 2005

41. Health Conditions And Diseases Genetic Disorders Coffin Lowry Syndrome
Top Health Conditions and Diseases Genetic Disorders Coffin LowrySyndrome (5). Top Web Sites coffin lowry syndrome An in
http://www.pastconnect.com/odp/directory/Health/Conditions_and_Diseases/Genetic_
Sponsored Links What are you looking for? the entire directory only in Genetic_Disorders/Coffin_Lowry_Syndrome Popular Categories Popular Searches Recent Categories Recent Searches ... Genetic Disorders : Coffin Lowry Syndrome Top Web Sites: Coffin Lowry Syndrome - An in depth article by Terry Patterson along with some images, hosted by Missouri Southern State College.
Coffin-Lowry Syndrome Foundation
- Information about the organization as well as CLS. Includes FAQs, news, links, parent and foundation contact details.
National Library of Medicine: Coffin-Lowry Syndrome (CLS)
- A table showing the synonyms, a summary and major features.
NINDS: Coffin Lowry Syndrome
- Information sheet compiled by the National Institute of Neurological Disorders and Stroke.
NORD: Coffin Lowry Syndrome
- General information about this syndrome, its alternative names and further resources.
Try other search sites: Coffin Lowry Syndrome " search on: All the Web AltaVista Gigablast Google USENET ... Yahoo Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Powered by ODP++

42. Coffin-Lowry Syndrome (CLS)
A table showing the synonyms, a summary and major features.
http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome238.html
Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
View the Full Record
Syndrome Coffin-Lowry syndrome (CLS) Synonyms Coffin syndrome 2 Coffin-Siris-Wegienka syndrome soft hands syndrome Summary Mental and somatic retardation in association with characteristic facies, large soft hands, and various bone abnormalities. A variant syndrome consists of growth and mental retardation, nail hypoplasia, hirsutism, and coarse facies with a large mouth, macroglossia, and bushy eyebrows. Major Features Head and neck: Midfacial hypoplasia, prominent forehead, flat occiput, prominent supraorbital ridges, and mandibular prognathism with relative maxillary retrognathia, in association with ear, nose and eye anomalies give the face a characteristic appearance. Thickened calvaria, large anterior fontanel, and delayed suture closing. Ears: Prominent pinnae. Eyes: Hypertelorism, downslanting palpebral fissures, and blepharoptosis. Nose: Large nose with flared alae and broad base and elongated philtrum. Mouth and oral structures: Large mouth, thick lips, open pouting mouth, and furrowed tongue. Malocclusion, absent or abnormal permanent incisors, and frequent periodontal disease with tooth loss.

43. Welcome
Information about the organization as well as CLS. Includes FAQs, news, links, parent and foundation contact details.
http://clsfoundation.tripod.com/
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44. Coffin-Lowry Syndrome
coffinlowry syndrome information and resources, genetic information, support groups coffin-lowry syndrome. coffin-lowry syndrome Foundation. c/o Mary Hoffman
http://www.kumc.edu/gec/support/coffin_l.html
Coffin-Lowry syndrome
Coffin-Lowry Syndrome Foundation
c/o Mary Hoffman
3045 255th Avenue S.E.
Sammamish, WA 98075
Phone: 425-427-0939 after 5:30 p.m. weekdays PST or weekends
E-mail: CLSFoundation@yahoo.com
Web Site: http://clsfoundation.tripod.com
Also See: To locate a genetic counselor or clinical geneticist: Revised April 6, 2001
Genetic Societies
Clinical Resources Labs Clinics ... Search
Genetics Education Center
Debra Collins, M.S. CGC
, Genetic Counselor, dcollins@kumc.edu
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45. Welcome
coffinlowry syndrome Foundation, a parent support group for families affected by coffin-lowry syndrome. Welcome to The coffin-lowry syndrome Foundation Home Page a clearinghouse for information on coffin-lowry syndrome (CLS), and to provide families affected by coffin-lowry
http://clsf.info/
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46. Coffin-Lowry Syndrome Foundation Welcome Page
The coffinlowry syndrome Foundation Web Site has moved. The new location is http//www.clsf.info. Welcometo The coffin-lowry syndrome Foundation Home Page.
http://clsfoundation.tripod.com/Welcome.htm
Welcome
The Coffin-Lowry Syndrome Foundation Web Site has moved.
The new location is http://www.clsf.info
Thank you for your patience.
Welcome to The Coffin-Lowry Syndrome Foundation Home Page. The purpose of this web site is to provide a clearinghouse for information on Coffin-Lowry Syndrome (CLS), and to provide families affected by Coffin-Lowry syndrome a general forum in which to exchange information, ideas and advice. CLSF provides family matching services, telephone support, an informational database and publishes a newsletter, CLSF News. The newsletter is available in hard-copy and on this web site. CLSF is a non-profit organization and is funded solely by donations and change I find under the couch cushions. Contact CLSF at 425-427-0939 M-F after 6pm PST or at CLSFoundation@yahoo.com. Coffin-Lowry Syndrome Foundation Attn: Mary C. Hoffman 3045 255th Avenue S.E. Sammamish, WA 98075 ".....we can reject everything else: religion, ideology, all received wisdom. But we cannot escape the necessity of love and compassion... This, then, is my true religion, my simple faith. In this sense, there is no need for temple or church, for mosque or synagogue, no need for complicated philosophy, doctrine or dogma. Our own heart, our own mind, is the temple. The doctrine is compassion. Love for others and respect for their rights and dignity, no matter who or what they are: ultimately these are all we need. So long as we practice these in our daily lives, then no matter if we are learned or unlearned, whether we believe in Buddha or God, or follow some other religion or none at all, as long as we have compassion for others and conduct ourselves with restraint out of a sense of responsibility, there is no doubt we will be happy." His Holiness the Dalai Lama

47. Coffin-Lowry Syndrome Information Diseases Database
coffinlowry syndrome, Disease Database Information Sponsors Contact Previous Page. coffin-lowry syndrome Information. coffin-lowry syndrome Definition(s) via UMLS ..Code translations
http://www.diseasesdatabase.com/sieve/item1.asp?glngUserChoice=2934

48. Introduction: Coffin-Lowry Syndrome - WrongDiagnosis.com
Introduction to coffinlowry syndrome as a medical condition including symptoms,diagnosis, misdiagnosis, treatment, prevention, and prognosis.
http://www.wrongdiagnosis.com/c/coffin_lowry_syndrome/intro.htm
Diseases IMPORTANT! Use of this site is subject to our and Home
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Current chapter: Coffin-Lowry syndrome Next sections Basic Summary for Coffin-Lowry syndrome Prevalence and Incidence of Coffin-Lowry syndrome Prognosis of Coffin-Lowry syndrome Causes of Coffin-Lowry syndrome ... Symptoms of Coffin-Lowry syndrome Next chapters: Coma Persistent Vegetative State Corticobasal Degeneration Cytomegalic Inclusion Body Disease ... Feedback
Introduction: Coffin-Lowry syndrome
Coffin-Lowry syndrome: Rare genetic condition causing various abnormalities. Coffin-Lowry syndrome: Coffin-Lowry syndrome is a rare genetic disorder characterized by craniofacial (head and facial) and skeletal abnormalities, mental retardation, short stature, and hypotonia. Contents for Coffin-Lowry syndrome: Footnotes: 1. excerpt from

49. Health Library -
SelfHelp Resources. Information about national and local self-help organizations and support groups. coffin-lowry syndrome. Self Help Clearinghouse. The coffin-lowry syndrome Foundation. International network. clearinghouse for information on coffin-lowry syndrome. Forum for exchanging experiences
http://www.yalenewhavenhealth.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=sh

50. Inheritance And Genetics Of Coffin-Lowry Syndrome - WrongDiagnosis.com
Inheritance and Genetics of coffinlowry syndrome includingheritability, family history, and inheritance patterns.
http://www.wrongdiagnosis.com/c/coffin_lowry_syndrome/inherit.htm
Diseases Coffin-Lowry syndrome IMPORTANT! Use of this site is subject to our and Home
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Search: We show you all these ads in order to provide this free site; give your feedback WrongDiagnosis TM Premium Report: Diabetes Diagnosis and Misdiagnosis Available Now!
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Current chapter: Coffin-Lowry syndrome Next sections Treatments for Coffin-Lowry syndrome Statistics about Coffin-Lowry syndrome Next chapters: Coma Persistent Vegetative State Corticobasal Degeneration Cytomegalic Inclusion Body Disease ... Feedback
Inheritance and Genetics of Coffin-Lowry syndrome
About inheritance and genetics: Inheritance of Coffin-Lowry syndrome refers to whether the condition is inherited from your parents or "runs" in families. The level of inheritance of a condition depends on how important genetics are to the disease. Strongly genetic diseases are usually inherited, partially genetic diseases are sometimes inherited, and non-genetic diseases are not inherited. For general information, see Introduction to Genetics Inheritance of Coffin-Lowry syndrome: X-linked dominant diseases are usually inherited, though rare cases of

51. COFFIN-LOWRY SYNDROME
Features Listed For coffinlowry syndrome. McKusick 303600. Coarse facialfeatures; Deafness, sensorineural; Delayed bone age; Flat malar region;
http://www.hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?328

52. Coffin-Lowry Syndrome
The coffinlowry syndrome Foundation. coffin-lowry syndrome The coffin-lowrysyndrome Foundation International network. Founded 1991.
http://my.webmd.com/hw/raising_a_family/shc29cof.asp
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Health Topics Symptoms ... The Coffin-Lowry Syndrome Foundation Coffin-Lowry Syndrome The Coffin-Lowry Syndrome Foundation International network. Founded 1991. Serves as a clearinghouse for information on Coffin-Lowry syndrome. Forum for exchanging experiences, advice and information with other CLS families. Seeks to become a visible group in the medical, scientific, educational, and professional communities in order to facilitate referrals of newly diagnosed individuals, and to encourage medical and behavioral research in order to improve methods of social integration of CLS individuals. Maintains mailing list of families and professionals. Provides newsletter, family support, informational packet. WRITE: Coffin-Lowry Syndrome Foundation c/o Mary C. Hoffman, Chair

53. Coffin-Lowry Syndrome
Founded 1991. Serves as a clearinghouse for information on coffinlowrysyndrome. coffin-lowry syndrome. The coffin-lowry syndrome Foundation.
http://www.bchealthguide.org/kbase/shc/shc29cof.htm
document.write(''); var hwPrint=1; var hwDocHWID="shc29cof"; var hwDocTitle="Coffin-Lowry Syndrome"; var hwRank="1"; var hwSectionHWID="shc29cof"; var hwSectionTitle=""; var hwSource="cn6.0"; var hwProdCfgSerNo="wsh_html_031_s"; var hwDocType="SHC";
Self Help Clearinghouse
Coffin-Lowry Syndrome
The Coffin-Lowry Syndrome Foundation
International network. Founded 1991.
Serves as a clearinghouse for information on Coffin-Lowry syndrome. Forum for exchanging experiences, advice and information with other CLS families. Seeks to become a visible group in the medical, scientific, educational, and professional communities in order to facilitate referrals of newly diagnosed individuals, and to encourage medical and behavioral research in order to improve methods of social integration of CLS individuals. Maintains mailing list of families and professionals. Provides newsletter, family support, informational packet.
WRITE:
Coffin-Lowry Syndrome Foundation
c/o Mary C. Hoffman, Chair
3045 255th Avenue S.E.

54. FSP Syndromes
coffinlowry syndrome l Ribosomal Protein S6 kinase, 90 kD, Polypeptide3 ; Xp22.2-p22.1; Dominant Genetics Multiple mutation types
http://www.neuro.wustl.edu/neuromuscular/spinal/fsp.html

Front
Search Index Links ... Patient Info
FAMILIAL SPINAL CORD SYNDROMES
General principles
Familial Spastic Paraplegia ( SPG

Dominant

: Atlastin; 14q11
: Spastin; 2p22
SPG 12q

Recessive

: Paraplegin; 16q24
(Troyer): Spartin; 13q12.3
(Mast): Maspardin; 15q22 Infantile onset : Alsin; 2q33 X-linked : Proteolipid protein; Xq22 Other: Deafness Familial Spastic Paraplegia +... Ataxia CNS Ocular PNS ... Systemic Disorders Leukodystrophies Adrenomyeloneuropathy : ALDP; Xq28 Adult-onset Krabbe : GalC; 14q31 MLD : Arylsulfatase A; 22q13 Other spinal cord syndromes Syndromes AAA syndrome : Aladin; 12q13 Adrenomyeloneuropathy : ALDP; Xq28 Alexander : GFAP; 17q21; Dominant Alzheimer's : Presenilin 1; 14q24; Dominant Arnold-Chiari Malformation (SPG9): 10q23; Dominant Cavanagh's Cerebral palsy-Symmetrical Cerebrotendinous xanthomatosis : Cytochrome 450; 2q33 Charlevoix-Saguenay : Sacsin; 13q11 Deafness : X-linked DOPA-responsive dystonias DRPLA : DRPLA protein; 12p13; Dominant Episodic ataxia : 1p; Dominant Evans Fitzsimmons syndrome Friedreich ataxia : FRDA; 9q13 Hereditary Motor Syndromes HHH syndrome HMSN 5 : Dominant : ARX; Xp22

55. GeneReviews: Coffin-Lowry Syndrome
Your browser does not support HTML frames so you must view coffinlowry Syndromein a slightly less readable form. Please follow this link to do so.
http://www.genetests.org/profiles/cls
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56. ORPHANET - Maladies Rares - Médicaments Orphelins
Translate this page Version pour Impression, MALADIE coffin-lowry, syndrome de, CIM Q87.8,Le syndrome de coffin-lowry (CLS) est une maladie génétique
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=192

57. ORPHANET® : Coffin-Lowry, Syndrome De
Translate this page ORPHANET. Accès à la base de données Orphanet. coffin-lowry, syndromede. Accès direct aux détails Résumé Le syndrome de coffin
http://www.orpha.net/static/FR/coffinlowry.html
Accès à la base de données Orphanet
Coffin-Lowry, syndrome de
Accès direct aux détails Résumé
Signes de la maladie
  • AILES DU NEZ EPAISSES / LARGES
  • DIAPHYSES ANOMALIE
  • DISQUE INTERVERTEBRAL ANOMALIE
  • DOIGTS PHALANGE DISTALE LARGE/DEVIEE
  • FENTE PALPEBRALE ANTIMONGOLOIDE
  • FRONT ETROIT/RETRACTION TEMPORALE
  • HYPERTELORISME
  • LEVRE INFERIEURE EVERSEE/TOMBANTE
  • LEVRES EPAISSES
  • LEVRES PROEMINENTES
  • NARINES ANTEVERSEES
  • NEZ LARGE/ARETE NASALE LARGE
  • PETITE TAILLE / NANISME
  • RACINE DU NEZ LARGE
  • REBORD ORBITAIRE SAILLANT
  • RETARD MENTAL SEVERE
  • SCOLIOSE
  • TRANSMISSION AUTOSOMIQUE DOMINANTE
  • ANODONTIE/OLIGODONTIE
  • ANOMALIE DU COU ET CAGE THORACIQUE
  • CRANE:VOUTE EPAISSIE/DENSITE AUGMENTEE
  • DENTS MAL IMPLANTEES
  • HYPERLAXITE LIGAMENTAIRE
  • MACROCEPHALIE
  • MICRODONTIE TOTALE OU PARTIELLE
  • ONGLES ABSENTS / PETITS (MAINS)
  • PALAIS OGIVAL/ETROIT
  • POMMETTES PLATES/MALAIRE HYPOPLASIE
  • PROGNATHISME
  • RETARD MENTAL MODERE / LEGER
  • AGE OSSEUX RETARD
  • CYPHOSE
  • MICROCEPHALIE
  • PECTUS EXCAVATUM
  • PHILTRUM LONG
Mise à jour : 01/06/2004
Accès à la base de données Orphanet

58. Coffin-Lowry Syndrome - Medical Dictionary Definitions Of Popular Medical Terms
MedicineNet Home MedTerms medical dictionary AZList coffinlowry syndrome. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=20785

59. Syndrome, Coffin-Lowry - Medical Dictionary Definitions Of Popular Medical Terms
MedicineNet Home MedTerms medical dictionary AZList syndrome, coffinlowry. Advanced Search.
http://www.medterms.com/script/main/art.asp?articlekey=20786

60. Coffin-Lowry Syndrome Information Diseases Database
coffinlowry syndrome may cause or feature Medical information linkscoffin-lowrysyndrome specific sites. Medical dictionary, library and
http://www.diseasesdatabase.com/ddb2934.htm
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