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         Ectodermal Dysplasia:     more books (15)
  1. Freire-Maia Ectodermal Dysplasias- A Clinical an D Genetic Study by N FREIRE-MAIA, 1985-02-06
  2. Ectrodactyly-ectodermal dysplasia-cleft syndrome
  3. Ectrodactyly-ectodermal dysplasia-clefting syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Kathleen, MS, CGC Fergus, 2005
  4. Children with ectodermal dysplasias.: An article from: Journal of School Health by Virginia L. Maturen, 1998-05-01
  5. Hypohidrotic Ectodermal Dysplasia - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-17
  6. ECTRODACTYLY-ECTODERMAL DYSPLASIA-CLEFTING SYNDROME IN AN INFANT WITH A VENTRICULAR SEPTAL DEFECT.: An article from: Georgia Journal of Science by Byron A. Brown, Joshua E. Lane, et all 2000-09-22
  7. Ectodermal dysplasia: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Jennifer, MS, CGC Roggenbuck, 2005
  8. Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome (EEC) Medical Guide by Qontro Medical Guides, 2008-07-09
  9. Oligodontia and ectodermal dysplasia - on signs, syptoms, genetics, and outcomes of dental treatment by Birgitta Bergendal, 2010-05
  10. Recent advances in ectodermal dysplasias (Birth defects, original article series)
  11. Recent Advances in Ectodermal Dysplasias (Birth Defects Original Article Series) by Carlos F. Salinas, John M. Opitz, 1988-09
  12. Charley's story by Mary Kaye Richter, 2000
  13. Adams-Oliver syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Amy, MS, CGC Vance, 2005
  14. Goltz syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005

81. ILDS: ICD-10 - By Disorder [X Linked Hypohidrotic Ectodermal Dysplasia - Xray Ne
ICD Code Disorder, Q82400 X linked hypohidrotic ectodermal dysplasia, Q801X linked ichthyosis, H026 Xanthelasma, D76301 Xanthogranuloma juvenile,
http://www.ilds.org/icd10/bydisorder/X.html
Application to Dermatology of ICD-10 Alphabetized by Disorder starting with X:
Return to Alphabetical listing...
ICD Code: Disorder X linked hypohidrotic ectodermal dysplasia X linked ichthyosis Xanthelasma Xanthogranuloma juvenile Xanthogranuloma necrobiotic Xanthoma disseminatum Xanthoma eruptive Xanthoma hypercholesterolemic Xanthoma hyperlipidemic Xanthoma plane Xanthoma tendinous Xanthoma tuberous Xanthomatosis cerebrotendinous Xanthomatosis diffuse normolipemic plane Xanthomatosis with sitosterolemia Xanthosiderohistiocytosis disseminated Xeroderma acquired Xeroderma due to vitamin A deficiency Xeroderma pigmentosum Xerosis cutis Xerostomia Xray alopecia Xray necrosis Return to Alphabetical listing... Contact: info@ilds.org ILDS

82. ILDS: ICD-10 - By Code [Q80809 - Q82801]
Q82400 Hypotrichosis in anhidrotic ectodermal dysplasia, Q82400 Anhidroticectodermal dysplasia, Q82400 Hypohidrotic ectodermal dysplasia,
http://www.ilds.org/icd10/bycode/Q-02.html
Application to Dermatology of ICD-10 Alphabetized by ICD Code starting with Q:
Return to Alphabetical listing...
ICD Code: Disorder Ichthyosis vera Alligator skin Ichthyosis congenita (NOS) Keratosis congenita (NOS) Disease Koebner's Koebner's disease Epidermolysis bullosa simple generalised Epidermolysis bullosa simple Koebner Epidermolysis bullosa simple Gedde Dahl Epidermolysis bullosa simple Cockayne Epidermolysis bullosa simple of hands and feet Syndrome Weber Cockayne Weber Cockayne syndrome Ogna variant of epidermolysis bullosa simplex Epidermolysis bullosa simple Ogna Syndrome Herlitz Herlitz syndrome Epidermolysis bullosa Herlitz Epidermolysis bullosa lethal junctional Epidermolysis bullosa recessive generalised dystrophic Epidermolysis bullosa recessive inverse dystrophic Epidermolysis bullosa recessive non-mutilating dystrophic Epidermolysis bullosa recessive localised dystrophic Syndrome Cockayne Touraine Epidermolysis bullosa dystrophic cockayne touraine Cockayne Touraine syndrome Dominant dystrophic epidermolysis bullosa Epidermolysis bullosa albopapuloid Hallopeau Siemens syndrome Syndrome Hallopeau Siemens Herpetiform epidermolysis bullosa Epidermolysis bullosa Dowling Meara Epidermolysis bullosa simple herpetiform Epidermolysis bullosa Pasini Epidermolysis bullosa non-lethal junctional generalised Epidermolysis bullosa non-lethal junctional inverse Epidermolysis bullosa non-lethal junctional localised Disease Goldscheider's Epidermolysis bullosa progressive junctional

83. Arch Ophthalmol -- Page Not Found
119;18661867, December 2001, Bilateral Multiple Eyelid Apocrine Hidrocystomasand ectodermal dysplasia, Uma Mallaiah, FRCS; Jane Dickinson, MRCP, FRCOphth.
http://archopht.ama-assn.org/issues/v119n12/ffull/epe10007-1.html
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery MSJAMA Science News Updates Meetings Peer Review Congress
The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"

84. CyberSpace Search!
SEARCH THE WEB. Results 1 through 3 of 3 for ectodermal dysplasia.
http://www.cyberspace.com/cgi-bin/cs_search.cgi?Terms=ectodermal dysplasia

85. Affected By Ectodermal Dysplasia
hi, i am affected by ectodermal dysplasia haywells syndrome. mychildren are also affected. i'd like to communicate with others
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86. Welcome To ENH.org - Health Encyclopedia: Ectodermal Dysplasia
ectodermal dysplasia. Alternative Names Anhidrotic ectodermal dysplasia.Causes, incidence, and risk factors There are several different
http://www.enh.org/Encyclopedia/ency/article/001469.asp

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Ectodermal dysplasia
Disease Injury Nutrition Poison ... Z Definition: A hereditary condition characterized by abnormal development of the skin and associated structures (hair, nails and teeth, and sweat glands).
Alternative Names: Anhidrotic ectodermal dysplasia
Causes, incidence, and risk factors: There are several different types of ectodermal dysplasia of which X-linked anhidrotic ectodermal dysplasia is the most common. This condition affects only males. An autosomal dominant form exists in which females and males are equally affected and is symptomatically almost identical to the X-linked form of the disease. Multiple genes have been discovered to cause ectodermal dysplasias.
Ectodermal dysplasia may affect, to varying degrees, all of the structures associated with the development of the skin. Absent or decreased sweating in people with anhidrotic ectodermal dysplasia is caused by absence of sweat glands. Affected children have difficulty controlling fevers and mild illness may produce extremely high fevers, because of absent temperature regulation by sweating . Affected adults are unable to tolerate a warm environment and require special measures to maintain a normal body temperature
Mucus membrane involvement results in chronic nasal infections with foul-smelling discharge and increased respiratory infections. Hair may be absent or very scanty. The skin is thin with light pigmentation. Teeth develop abnormally and many teeth are missing.

87. 1993: Hypohidrotic Ectodermal Dysplasia And Hypomelanosis Of Ito In A Girl With
Hypohidrotic ectodermal dysplasia and Hypomelanosis of Ito in a girl with a denovo t(X;13)(q13;p11.2). SJ Orlow 1 , R. Marion 2 , C. Duncan 3 , H. Gu 3 , M
http://www.faseb.org/genetics/ashg99/f1993.htm
Program Nr: 1993 Hypohidrotic ectodermal dysplasia and Hypomelanosis of Ito in a girl with a de novo t(X;13)(q13;p11.2). S.J. Orlow , R. Marion , C. Duncan , H. Gu , M. Genovese , E. Jenkins , A. Shanske 1) Dermatology, NYU Medical Center, New York, NY; 2) Pediatrics, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY; 3) Institute for Basic Research, Staten Island, NY.
We conclude that our patient is a fully manifesting female with HED because the translocation affects the EDA1 gene.Functional disomy has been proposed as a likely mechanism because of the skewed X-inactivation observed in most cases.PCR analysis of DNA extracted from uncultured cells show that a more balanced pattern of inactivation can be observed in these cells.Partial functional disomy in the fibroblast cell lineage may also be responsible for the HI in our patient.

88. 794: Hypothyroidism In An Infant With Ectodermal Dysplasia And Cleft Lip And Pal
Program Nr 794 Hypothyroidism in an infant with ectodermal dysplasiaand cleft lip and palate. J. DiMartinoNardi 1 , A. Palomba
http://www.faseb.org/genetics/ashg99/f794.htm
Program Nr: 794 Hypothyroidism in an infant with ectodermal dysplasia and cleft lip and palate. J. DiMartino-Nardi , A. Palomba , A. Shanske 1) Pediatrics, Montefiore Medical Center, Bronx, NY; 2) Pediatrics, Bronx Municipal Hospital Center, Bronx, NY. The association of ectodermal dysplasia (ED) and clefting deformity is well known and has been reported in patients with a variety of disorders.A combination of oral clefting, ectropion and ED are the cardinal features of the blepharocheilodontic syndrome.Reports of ED and hypothyroidism are rare.We recently evaluated an infant with ED, cleft lip and palate and primary hypothyroidism.
AK was the 3.8 kg product of an uneventful pregnancy born to consanguineous Pakistani parents with a left-sided cleft lip and palate,ectropion,and dermoid cysts on the face and scalp.He was admitted at 4 months of age to our hospital because of respiratory distress.His physical examination at that time revealed a malnourished hypotonic infant with the additional findings of ankyloglossia, a large fontanelle, sparse lashes, absent eyebrows and normal nails. His length was 59 cm, weight 4 kg, and HC was 38.5 cm.The anterior fontanelle measured 5 by 4.5 cm and the primary dentition had not yet erupted. Imaging studies revealed a pericardial effusion, dilated loops of bowel, the bone age of a newborn, the absence of tooth follicles, and a normal MRI of the head.Laboratory investigation revealed a normal male karyotype,a TSH greater than 700 m U/ml,a barely detectable level of T

89. JAX®Mice Database - Mouse/Human Gene Homologs: Hypohidrotic Ectodermal Dysplasi
JAX®MICE Database Mouse/Human Gene Homologshypohidrotic ectodermal dysplasia List.
http://jaxmice.jax.org/jaxmicedb/html/model_1010.shtml

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(link to Data Sheet) Strain Type Standard Supply A w-J .CBy- Eda ... Ta-By Level 5 Cryopreserved. See Options 1, 2 and 3 listed in Supply Note field on data sheet. a a Edaradd cr Level 4: Up to 3 breeder pairs or 6 individual mice per order total; 1 order at a time. Expected delivery for most strains is 1 to 3 months. Call to inquire about ordering greater quantities. A w-J A-Eda Ta ... /O Level 4: Up to 3 breeder pairs or 6 individual mice per order total; 1 order at a time. Expected delivery for most strains is 1 to 3 months. Call to inquire about ordering greater quantities. C3H/HeJ- Eda Ta-5J Level 5 Cryopreserved. See Options 1, 2 and 3 listed in Supply Note field on data sheet. A w-J -Eda Ta-6J Level 4: Up to 3 breeder pairs or 6 individual mice per order total; 1 order at a time. Expected delivery for most strains is 1 to 3 months. Call to inquire about ordering greater quantities. A w-J -Eda Ta ... Tfm Level 5 Cryopreserved. See Options 1, 2 and 3 listed in Supply Note field on data sheet.

90. Search By Disease
4 ectodermal dysplasia 1, anhidrotic (ED1). 5 ectodermal dysplasia 3, anhidrotic,autosomal dominant (EDA3). 6 ectodermal dysplasia, anhidrotic (EDA).
http://www.eddnal.com/directory/disease.php?letter=E

91. Hypohidrotic Ectodermal Dysplasia, EDA µL¦½¯g
The summary for this Chinese (Traditional) page contains characters that cannot be correctly displayed in this language/character set.
http://www.genephile.com.tw/Tests/EDA.htm
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EDA ­P¯f¾÷Âà¡J 80%±wªÌ¦bED1°ò¦]µo¥Í¬ðÅÜ¡A¾É­P²Ó­M½¤³J¥Õ¤Wªº Ectodysplasin-A ³J¥Õ¯Ê³´¡AµLªk±µ¨üTumor necrosis factor(TNF)¤§½Õ±±¡A¾É­P­ÓÅé¥Ñ¥~¥Ö¼h°_·½ªº¾¹©x²§±`¡C ÀË´ú¶µ¥Ø¡J 1. ED1°ò¦]¡A¦X­p9­Ó Exon¡C
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92. Congenital, Hereditary, And Neonatal Diseases And Abnormalities
Comprehensive list of links from Karolinska Institutet, Sweden.Category Health Nursing Specialties Neonatal...... ectodermal dysplasia The US Nat'l Foundation for ectodermal dysplasias;The ectodermal dysplasia Society; About Hypohidrotic (Anhydrotic
http://www.mic.ki.se/Diseases/c16.html
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
(including Pediatrics)
Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Alphabetical List of Diseases

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93. Ectodermal Dysplasia - General Practice Notebook
medical information from General Practice Notebook. ectodermal dysplasia.ectodermal dysplasia is a generic term refering to abnormalities
http://www.gpnotebook.co.uk/cache/2020278292.htm
ectodermal dysplasia Ectodermal dysplasia is a generic term refering to abnormalities in the formation of the skin and associated structures, such as hair, nails, teeth, and skin glands.
Click here for more information...

94. NTvT - Ectodermal Dysplasia
Syndromes 17. Hypohidrotic ectodermal dysplasia. pict. 2b Orthopantomogramand 'tracing' of the dentition with only 13 teeth and 1 milktooth.
http://www.ntvt.nl/e107ectdp12.htm
Syndromes 17
Hypohidrotic ectodermal dysplasia pict. 2b: Orthopantomogram and 'tracing' of the dentition
with only 13 teeth and 1 milk-tooth. NTvT 107:12-14.

95. Katalog - Wirtualna Polska
Serwis Katalog w Wirtualna Polska S.A. pierwszy portal w Polsce.
http://katalog.wp.pl/DMOZ/Health/Conditions_and_Diseases/Genetic_Disorders/Ectod
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