81. Health Library - organizations and support groups. apert syndrome. Self Help Clearinghouse. apert syndrome Pen Pals. National network. Founded 1992.Group correspondence http://12.42.224.152/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29ape

82. Apert Syndrome Associated With Brain Abscess At Birth - Eurorad - Clinical Case teaching files,radiology,apert syndrome associated with brain abscess at birth,Female infant presenting with abnormal facial appearance, fusion of the hands http://www.eurorad.org/case.cfm?uid=1422

83. Short Description Of Cell Lines. Pathology: Apert Syndrome #101200 Version 4.200205, Short description of cell lines. Pathology apert syndrome 101200 OMIM record. By selecting the cell line name http://www.biotech.ist.unige.it/cldb/pat312.html

Version Short description of cell lines. Pathology: Apert syndrome OMIM record By selecting the cell line name , you will receive the detailed description of the cell line By selecting one of the terms between parentheses, you will receive the list of all relevant cell lines You can search any term of the list by using the 'Find' utility of your browser human, Caucasian amnion GGB By Beatrice...

84. Apert Syndrome Pen Pals apert syndrome Pen Pals. PO Box 115 Providence, RI 02901 Conditions apert syndrome; Acrocephalosyndactyly, Type I. Hours Answered MF, 930830 Voicemail yes. http://www.geneticalliance.org/diseaseinfo/displayorganization.html?orgname=Aper

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87. Qango : Health: Diseases And Conditions: A: Apert Syndrome Qango Directory apert syndrome all of Qango only this category Options Help. Home Health Diseases and Conditions A apert syndrome, Suggest a Site. http://www.qango.com/dir/Health/Diseases_and_Conditions/A/Apert_Syndrome/

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88. Apert Syndrome From Linkspider UK Health Directory apert syndrome by Linkspider UK, apert syndrome links and apert syndrome topics from our Health directory. Directory Topic apert syndrome assoicated to Health. http://linkspider.co.uk/Health/SupportGroups/ConditionsandDiseases/FacialDiffere

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89. Apert's Syndrome apert s syndrome. apert s syndrome is a relatively uncommon craniofacial condition. It occurs with a frequency of one in 160,000 live births. http://www.worldcf.org/cran_3c1.html

World Craniofacial Foundation 7777 Forest Lane, Ste C-621 P.O. Box 515838 Dallas, TX 75251-5838 fax 972-566-3850 worldcf@worldnet.att.net Apert's Syndrome Apert's syndrome is a relatively uncommon craniofacial condition. It occurs with a frequency of one in 160,000 live births. The condition may be inherited with a frequency of 50% in the off-spring of an affected adult, or may develop as a spontaneous mutation. Characteristics The physical features of this condition were described by Frederick Apert in 1942 and include: A tower-shaped skull due to craniosynostosis An under-developed mid-face leading to recessed cheek bones and prominent eyes. Malocclusion Limb abnormalities such as webbing of the middle digits of the hands and feet Some other features commonly seen in this condition are visual disturbances related to an imbalance of the muscles that move the eyes, a hearing loss due to recurrent ear infections, and varying degrees of acne. There can be a reduced intellectual capacity in some individuals but there are some children with this condition who have normal intelligence. Children with Apert's have fusion of the bones of their fingers and toes, characterized by the "mitten-like appearance of their hands. This is called syndactyly. Cardiac and gastrointestinal malformations may be present in Apert's patients which have not been described for those individuals with other syndromes. Cause The basic cause of this is linked to a single gene alteration of Fibroblast Growth Factor. Their occurrence is sporadic and extremely rare. In most cases of Apert's, the deformity occurs from abnormal occurrence in the genes which cannot be traced to a specific cause. Usually, the parents are not affected and the risk for future children of that couple to have Apert's is minimal. The offspring of an Apert's patient have a 50-60% chance of inheriting the syndrome.

90. Apert's Syndrome (www.whonamedit.com) apert s syndrome A complex of craniofacial abnormalities caused by premature craniosynostosis, usually of the coronal suture, leading to turribrachycephaly http://www.whonamedit.com/synd.cfm/194.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Apert's syndrome Also known as: Apert's syndactyly Synonyms: Acrocephalosyndactylism, acrocephalosyndactyly type I, acrocephaly with syndactyly, acrocraniodysphalangia, acrodysplasia, syndactylic oxycephaly syndrome. Associated persons: Eugène Charles Apert Description: A complex of craniofacial abnormalities caused by premature craniosynostosis, usually of the coronal suture, leading to turribrachycephaly, associated with syndactyly and polydactyly. Cranial abnormalities are of the brachysphenocephalic type with high forehead, small nose, supraorbital horizontal groove, shallow orbits, antimongoloid palpebral fissures, hypoplastic maxilla, and narrow palate. Cleft palate may occur. Syndactyly is due to osseous fusion of the second and fourth fingers with a single nail and soft tissue fusion of the fourth or second to fifth, or of all toes, thus giving the hands and feet a mitten-like appearance. There may be also shortening of upper extremities, deformation of the pectoral girdle, and abnormalities of genitourinary, gastrointestinal, and cardiovascular systems. The syndrome is transmitted as an autosomal dominant trait.

91. Apert's Syndrome apert s syndrome,. Print this article, (Eugene apert, 1868–1940, French paediatrician), an autosomal dominant disorder characterized http://www.amershamhealth.com/medcyclopaedia/Volume III 1/APERTS SYNDROME.asp

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Apert's syndrome, (Eugene Apert, 1868–1940, French paediatrician), an autosomal dominant disorder characterized by closure of the sutures, hypoplasia of the midface, and syndactyly of both hands and feet. At birth affected infants also have an extensive midline calvarial defect. The calvaria is thin and undermineralized. Brachycephaly is seen after the first 4 years of life when the sagittal suture area closes. The child has small orbits, a hypoplastic maxilla and a small nasopharynx. In addition, the thumb is deviated and a complex osteocartilaginous syndactyly of the distal phalanges is seen. Abnormalities of the foot include syndactyly, a triangular first proximal phalanx, and progressive fusion of tarsal and metatarsal bones. Bone fusion may also be evident in other joints, including the cervical spine. (See acrocephalosyndactyly (III:1), Fig. 1 DR The Encyclopaedia of Medical Imaging Volume III:1 Contacts GE Healthcare Making Waves

92. Apert's Syndrome apert s syndrome,. Print this article, (Eugene apert, 18681940, French paediatrician), an autosomal dominant disorder characterized http://www.amershamhealth.com/medcyclopaedia/medical/Volume III 1/APERTS SYNDROM

Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Apert's syndrome, (Eugene Apert, 18681940, French paediatrician), an autosomal dominant disorder characterized by closure of the sutures, hypoplasia of the midface, and syndactyly of both hands and feet. At birth affected infants also have an extensive midline calvarial defect. The calvaria is thin and undermineralized. Brachycephaly is seen after the first 4 years of life when the sagittal suture area closes. The child has small orbits, a hypoplastic maxilla and a small nasopharynx. In addition, the thumb is deviated and a complex osteocartilaginous syndactyly of the distal phalanges is seen. Abnormalities of the foot include syndactyly, a triangular first proximal phalanx, and progressive fusion of tarsal and metatarsal bones. Bone fusion may also be evident in other joints, including the cervical spine. (See acrocephalosyndactyly (III:1), Fig. 1 DR The Encyclopaedia of Medical Imaging Volume III:1 Contacts GE Healthcare Making Waves

93. Apert S Syndrome apert s syndrome, Pediatric neurosurgery Specialty Center. figure patient with apert s syndrome. Return to uscneurosurgery.com Homepage. http://uscneurosurgery.com/glossary/a/aperts syndrome.htm

94. Apert's Syndrome Information Diseases Database apert s syndrome,Vogt cephalodactyly,Acrocephalosyndactyly syndrome type 1,Acrosphenosyndactylia,apertCrouzon disease, Disease Database Information. http://www.diseasesdatabase.com/ddb29300.htm

Diseases Database Index Sponsors Contact ... Previous Page Apert's syndrome Information Search 5 synonyms or equivalents were found. Apert's syndrome aka/or Vogt cephalodactyly aka/or Acrocephalosyndactyly syndrome type 1 aka/or Acrosphenosyndactylia aka/or Apert-Crouzon disease may cause or feature (Follow link for list) may be allelic with (Follow link for list) belong(s) to the category of (Follow link for list) Apert's syndrome: Definition(s) via UMLS Code translations and terms via UMLS Apert's syndrome: specific sites Send Apert's syndrome to medical search engines (JavaScript enabled browsers only) If your browser has no JavaScript you can still use these: Search using Internet medical databases Search using Internet search engines (non-specialist) We subscribe to the HONcode principles of the Health On the Net Foundation i-medicine.info - the evidence based medicine, informatics and audit portal Valid XHTML 1.0 Served 2004-06-02 08:53:49 Metadata Updated 2004-05-22

95. Apert's Syndrome apert s syndrome. DESCRIPTION Autosomal dominant mutation characterized by acrocephalosyndactyly and mental retardation. Usual course chronic; progressive. http://www.5mcc.com/Assets/SUMMARY/TP0076.html

Apert's syndrome DESCRIPTION: Autosomal dominant mutation characterized by acrocephalosyndactyly and mental retardation. Usual course - chronic; progressive. CAUSES: unknown probable early bridging of mesenchymal blastema probable early bridging of bone hypoplasia Synonyms: acrocephalosyndactyly ICD-9-CM: 755.55 acrocephalosyndactyly Author(s): Mark R. Dambro, MD

96. Dictionary Definition Of APERT'S SYNDROME Dictionary definition of apert S syndrome. Medical dictionary. Browse Dictionary by alphabet. 0 1 2 3 4 5 6 7 8 9 A B C D E F G H I http://www.dictionarybarn.com/APERTS-SYNDROME.php

Dictionary definition of APERT'S SYNDROME Browse Dictionary by alphabet A B C D ... Z Top Words AP projection AP24 apoptotic protease APA apache ... aphanisis Since it is usually autosomal dominant one or both parents also have the disorder. Surgery is used to correct skull and facial abnormalities. Inheritance: autosomal dominant. Please select first two letters of word you are looking for AA AB AC AD ... AZ fiSearchFormMaxSetId='AX006027'; Top Words aphanite aphanitic aphasia, broca aphasia, conduction ... Home Sponsored By: Georgia Hotels Guam Hotels Hawaii Hotels

97. Health Diary >> Bones And Joints >> Apert's Syndrome Home Bones and Joints apert s syndrome. apert s syndrome. http://www.healthdiary.com/story.php?id=11

98. Intro Screen... Skip Intro . http://members.aol.com/ApertSyn/

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