1. Dolicocephaly Home. Up. dolicocephaly. Sagittal Synostosis Homepage http//www.geocities.com http://www.medlina.com/dolicocephaly.htm

100 Hot Books 100 Hot CDs 100 Hot Videos 100 Hot DVDs ... Women's Health T he Web MEDLINA.com CDC WHO FDA NIH Search: All Products Books Magazines Popular Music Classical Music Video DVD Baby Electronics Software Outdoor Living Wireless Phones Keywords: CATEGORIES Home Up Dolicocephaly Sagittal Synostosis Homepage - http://www.geocities.com Information (including details of genetic research) and support for people affected by this condition. Craniosynostosis - http://www.kidsplastsurg.com Definition, description, diagnosis, treatment and support. Pictures included. Questions and Answers - Craniosyntosis - http://www.neurosurgery.org Frequently asked questions about craniosyntosis, patient and physician resources, and news. SUBCATEGORIES Up Search Now: info@medlina.com N ew Y ork C ity A merica M edica, I nc.

2. Birth Disorder Information Directory - S Saethre Chotzen Syndrome See Chotzen Syndrome. Sagittal Synostosis (Craniostenosis, Craniosynostosis, dolicocephaly, Scaphocephaly, Sagittal Craniostenosis http://www.bdid.com/defects.htm

HOME S Saal Bulas Syndrome (Ectrodactyly with Diaphragmatic Hernia and Corpus Callosum Agenesis) ectrodactyly diaphragmatic hernia corpus callosum agenesis Sabinas Brittle Hair Syndrome (Brittle Hair Mental Deficit) brittle hair mental deficit BRITTLE HAIR AND MENTAL DEFICIT Sackey Sakati Aur Syndrome (Pancytopenia with Multiple Congenital Anomalies) Aur syndrome Sacral Agenesis See Caudal Regression Syndrome Syndrome See Currarino Triad Saethre Chotzen Syndrome See Chotzen Syndrome Sagittal Synostosis (Craniostenosis, Craniosynostosis, Dolicocephaly, Scaphocephaly, Sagittal Craniostenosis, Sagittal Craniosynostosis) List of Sites Related Books Sakati Nyhan Syndrome See Acrocephalopolysyndactyly, Type III Salamon Syndrome (Woolly Hair with Hypotrichosis, Everted Lower Lip and Outstanding Ears) Woolly hair hypotrichosis everted lower lip outstanding ears WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS Saldino Noonan McCreanor Syndrome See Short Rib-Polydactyly Syndrome Sammartino Decreccio Syndrome (Corneal Dystrophy Ichthyosis Microcephaly Mental Retardation) Corneal dystrophy ichthyosis microcephaly mental retardation Sandhoff Disease (Type I is from birth, but some of these links include info on Type II and/or Adult Onset as well)

3. The Sudroid (Indo-African) Race The Sudroid (IndoAfrican) Race. The Sudran, or Sudroid, race refers to the aboriginal populations of India. dolicocephaly - dolicocephaly ( long-headedness ) is common amongst Sudras many are classed as hyperdolicocephalic. dolicocephaly is common amongst East Africans in general http://www.geocities.com/Athens/Ithaca/1335/Anthro/sud_afr.html

The Sudroid (Indo-African) Race The Sudran, or Sudroid, race refers to the aboriginal populations of India. Formerly widepread over all of India, they were displaced from most of Hindustan (North India) and virtually all of the Deccan by invading Aryans. Sudroid includes the following peoples: Sudroid Dravidoids (speakers of Dravidian languages) Untouchables or Avarans Antyajas/Dalits/SC Adivasis/ST Vedic Shudrs (Aryanized and enslaved blacks) They are a black race, closely related to the Africans and Australoids, as evident from - Black skin broad noses thick lips and wavy-curly hair Linguistically, all the languages are related. Genetically they are closely related This ends the basic section. The advanced section is below. The Sudran (Indo-African) Race Table of Contents The unity of Sudroids, Africoids and Australoids 1. Physiognomic Similarities 1.1 Black Skin 1.2 Nose Width (Nasal Index) 1.3 Wavy-Curly Hair and Thick Lips ... 6.3 Botanical 1. Physiognomy Black Skin The most evident similarity between Africans and Sudroids is their black skin colour. It often approaches deep black, and when shiny resemble tar. The Adi Dravidas (true Dravidians) of South India are black like the Africans with a slightly different hair texture [ Win.gen ]. Nasal Index The nose of Sudroids closely resembles that of Negroids and Australoids, being very broad. In both pure black African and pure Sudroid it is often as wide as it is broad, ie. the nasal index (ratio of width to height) is 100. By contrast Caucasians are fine-nosed. The Indo-Aryan is thus very similar to the European, possessing a fine nose, while the Sudroid is related to the Africans -

4. 22q13 Hypotonia, developmental delay, speech difficulties, macrocephaly, seizures, ptosis, epicanthal folds, high arched palate, dolicocephaly, lymphedema, mild http://www.22q13.com/geneticterms.html

Vocabulary related to Deletion 22q13 Hypotonia, developmental delay, speech difficulties, macrocephaly, seizures, ptosis, epicanthal folds, high arched palate, dolicocephaly, lymphedema, mild dilation of cerebral ventricles, dysplastic ears, delay in gross motor milestones, normal or accelerated growth, mild facial dysmorphic features, dolicocephaly, downslanting palpebral fissures, simian crease, and syndactyly. What does it mean? Hypotonia: decreased tone of the skeletal muscles characterized by weakness and "floppiness" Developmental delay: Unable to meet... Macrocephaly: large head for which the cause may be unknown. It is not the same as fluid on the brain, which is typically called hydrocephaly and may require a shunt. Speech Difficulties: Growling, low gutteral utterances. Seizures: There may be mild seizures in which the child "tunes out" but does not have any physical spasms. Ptosis: Drooping of the upper eyelid - in other words, the eyes may look partially shut as if they are ready to fall asleep. Wandering eye is usually referred to as strabismus. Epicanthal folds: The vertical fold of skin on the inner corner of the eye ( on each side of the nose) is excessive and covers the inner corner of the eye. This feature is typically seen in individuals with Down syndrome and it is also a normal characteristic in certain races, such as Asians - that is why Down syndrome was initially referred to as Mongolism - the epicanthal fold is a normal trait in people of Mongolia.

5. CHROMOSOME 22 CENTRAL - 22q13 Deletion high arched palate. dolicocephaly. lymphedema. mild dilitation of cerebral ventricles mild facial dysmorphic features. dolicocephaly. downslanting palpebral fisuures. simian crease http://www.nt.net/~a815/22q13.htm

22q13 DELETION (Phelan-McDermid Syndrome) Register to be put in contact with 22q13 families registered with C22C Post to our 22q deletion Interest Message Board VISIT THE 22q13 DELETION SYNDROME FOUNDATION WEBSITE Subscribe to 22q13 Powered by www.egroups.com Deletion of 22q13.3 is not as common as 22q11 deletion. The deletion occurs at the very end tip (The distal end) of Chromosome 22. Patients missing this part of chromosome 22 present similar features. Studies for 22q13.3 deletion are ongoing at the The University of Alberta Hospital under the direction of Heather McDermid. FAMILY CONTACT FOR 22q13 DELETION Randy Riddle 5501 Vista Sandia NE Albuquerque, NM 87111 telephone: 505-323-9574 e-mail: the5riddles@earthlink.net There is a support group specifically for 22q13 families. Contact: Mary C. (Katy) Phelan, Ph.D., FACMG Genetic Diagnostic Laboratory T.C. Thompson Children's Hospital 910 Blackford Street - Suite 401 MPB Chattanooga, TN 37403 Phone: 423-778-6279 Fax: 423-778-3164 email: PhelanK@erlanger.org Findings in patients have included (in no particular order): Hypotonia developmental delay speech difficulties macrocephaly seizures Ptosis Epicanthal folds high arched palate dolicocephaly lymphedema mild dilitation of cerebral ventricles dysplastic ears delay in gross motor milestones normal or accelerated growth mild facial dysmorphic features Dolicocephaly downslanting palpebral fisuures simian crease syndactyly 22q13 DELETION ARTICLE LIBRARY C22C HOME MEMBERSHIP FORM ABOUT C22C ... CONTACT US

6. Dolicocephaly Browse entry words starting with A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, dolicocephaly,. Print this article, http://www.amershamhealth.com/medcyclopaedia/medical/Volume VI 1/DOLICOCEPHALY.A

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 Dolicocephaly, elongated, narrow skull secondary to total or partial premature closure of the sagittal suture (see craniosynostosis ). The skull growth necessarily occurs at the coronal sutures and thus the frontal bones may be prominent. Also called scaphocephaly. GS The Encyclopaedia of Medical Imaging Volume VI:1 Contacts GE Healthcare Making Waves

7. Prader Willi Syndrome and infantile central hypotonia with poor suck, improving with age; failure to thrive; characteristic facial features with dolicocephaly, narrow bifrontal http://www.amershamhealth.com/medcyclopaedia/medical/Volume VI 1/PRADER WILLI S

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 Prader willi syndrome, (Andrea Prader, 20th century, Swiss paediatrician; Heinrich Willi, 19001971, Swiss paediatrician), a rare congenital anomaly due to a deletion of the long arm of chromosome 15. Clinical manifestations include: neonatal and infantile central hypotonia with poor suck, improving with age; failure to thrive; characteristic facial features with dolicocephaly, narrow bifrontal diameter, almond-shaped eyes and small mouth; hypogonadism. Skull radiographs show microcrania, small sella turcica and absent frontal sinuses. CT may show slight ventricular dilatation. GS The Encyclopaedia of Medical Imaging Volume VI:1 Contacts GE Healthcare Making Waves

8. WWW: Dolicocephaly All about dolicocephaly www from BigTome.com Sorry, no results found for "dolicocephaly". Put this Directory on Your Site! http://www.bigtome.com/big/page/Dolicocephaly

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9. Sagittal Synostosis (Craniostenosis, Craniosynostosis, Dolicocephaly, Scaphoceph HOME. Sagittal Synostosis (Craniostenosis, Craniosynostosis, dolicocephaly, Scaphocephaly, Sagittal Craniostenosis, Sagittal Craniosynostosis). http://www.bdid.com/sagittal.htm

HOME Sagittal Synostosis (Craniostenosis, Craniosynostosis, Dolicocephaly, Scaphocephaly, Sagittal Craniostenosis, Sagittal Craniosynostosis) scaphocephaly CRANIOSTENOSIS - PROTRUDING EYES (Includes Image) CRANIOSTENOSIS - MALE PROFILE (Includes Image) Craniofacial Surgery...David Herz, M.D. Sagittal Synostosis Homepage craniofacial diseases CRANIOSYNOSTOSIS ... Craniosynostosis (Includes Photos and a Diagram) Brynne and craniosynostosis CRANIOSYNOSTOSIS CRANIOSYNOSTOSIS, TYPE 1; CRS1 Craniosynostosis ... Isolated Craniosynostosis (Includes Photos) HOME

10. Dolicocephaly dolicocephaly, elongated, narrow skull secondary to total or partial premature closure of the sagittal suture (see http://www.amersham-health.com/medcyclopaedia/Volume VI 1/DOLICOCEPHALY.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 Dolicocephaly, elongated, narrow skull secondary to total or partial premature closure of the sagittal suture (see craniosynostosis ). The skull growth necessarily occurs at the coronal sutures and thus the frontal bones may be prominent. Also called scaphocephaly. GS The Encyclopaedia of Medical Imaging Volume VI:1 Contacts GE Healthcare Making Waves

11. DISEASE: Dolicocephaly DISEASE Sorry, no results found for dolicocephaly . http://disease.bigtome.com/big/page/Dolicocephaly

DISEASE: Sorry, no results found for "Dolicocephaly". Put this Directory on Your Site! Submit a Site Become an Editor

12. BigTome.com Rhinitis Retinitis Pigmentosa Cyrptococcosis Gastrointestinal Disorders Murmurs Peripheral Neuropathy Hidradenitis Suppurativa dolicocephaly SteinLeventhal http://disease.bigtome.com/bth/bt1_disease_1.shtml

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13. Omniseek: /Health /Consumer Support Groups /Facial Differences /Sagittal Synosto also known as scaphocephaly, dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis known as scaphocephaly or dolicocephaly, the sagittal suture closes early http://www.omniseek.com/srch/{26969}

News Sections Business Community Computing Directory ... Travel Search Engine Omniseek Multisearch Article Archives About AltaVista Ask Jeeves Euroseek Excite Google Goto HotBot Infoseek LookSmart Lycos Omniseek Snap Webcrawler Yahoo Don't forget to come back to this page and click the check mark to vote for a site! Health /Consumer Support Groups /Facial Differences /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 (http://www.geocities.com/HotSprings/6751/) Open Directory - Health: Consumer Suppor . . . Facial Differences: 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 b (dmoz.org/Health/Consumer_Support_Groups/Facial_Differences/Sagittal_Synostosis/)

14. Sagittal Synostosis Homepage Sagittal synostosis (also known as scaphocephaly, dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), is a condition in infants where the http://www.geocities.com/HotSprings/6751/

There are over 100 links "buried" in our site. We've put the top ones all in 1 place for your convenience. Click Here! Dig deep and learn more about this condition, surgical options, and the future. Recent genetics research estimates that sagittal synostosis appears in 1 in 4000 to 1 in 8500 live births, with a 2 - 6% chance of being hereditary. In other words, there is only a 1 in 133,333 to 1 in 850,000 chance of having two children with this rare condition. Well, our two children each have it. Our daughter, Shauna, was born in July, 1997. Although the doctors and literature available in 1994 advised us that sagittal synostosis is not genetic, we now believe otherwise. At one week of age, Shauna was also diagnosed with sagittal synostosis. She ended up having the surgery in November, 1997, when she was 15 weeks old. In June, 2002, we had a third child, Melanie. She is almost 2 years old and has shown no signs whatsoever of sagittal synostosis. She has a perfectly round head and has passed all her developmental milestones. It has been almost 10 years since our first child was diagnosed with sagittal sysnostosis and 7 years since our daughter had the surgery. Our 3 children are all happy and healthy. The issue never seems to come up because all our children "look normal". We are truly grateful to to doctors and staff at the Toronto Hospital for Sick Children, who performed the surgery on our children and have enabled them to lead happy, healthy, and normal lives.

15. Sagittal Synostosis Homepage synostosis (also known as scaphocephaly, dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), is http://www.geocities.com/sagittal.geo

There are over 100 links "buried" in our site. We've put the top ones all in 1 place for your convenience. Click Here! Dig deep and learn more about this condition, surgical options, and the future. Recent genetics research estimates that sagittal synostosis appears in 1 in 4000 to 1 in 8500 live births, with a 2 - 6% chance of being hereditary. In other words, there is only a 1 in 133,333 to 1 in 850,000 chance of having two children with this rare condition. Well, our two children each have it. Our daughter, Shauna, was born in July, 1997. Although the doctors and literature available in 1994 advised us that sagittal synostosis is not genetic, we now believe otherwise. At one week of age, Shauna was also diagnosed with sagittal synostosis. She ended up having the surgery in November, 1997, when she was 15 weeks old. In June, 2002, we had a third child, Melanie. She is almost 2 years old and has shown no signs whatsoever of sagittal synostosis. She has a perfectly round head and has passed all her developmental milestones. It has been almost 10 years since our first child was diagnosed with sagittal sysnostosis and 7 years since our daughter had the surgery. Our 3 children are all happy and healthy. The issue never seems to come up because all our children "look normal". We are truly grateful to to doctors and staff at the Toronto Hospital for Sick Children, who performed the surgery on our children and have enabled them to lead happy, healthy, and normal lives.

16. DO MEXICANS & OTHER LATINO'S CLAIM ASIAN BLOOD? dolicocephaly dolicocephaly ( long-headedness ) is common amongst Sudras. In fact, many are classed as hyperdolicocephalic. dolicocephaly http://boards.brownpride.com/showflat.php?Cat=&Board=social&Number=953953&page=0

17. Tricho Dento Osseous Syndrome fusion) of the fibrous joints between certain bones in the skull (craniosynostosis), causing the head to appear abnormally long and narrow (dolicocephaly). http://my.webmd.com/hw/raising_a_family/nord386.asp

var guid_source = ""; var guid_source_id = ""; //unused var encodedurl = ""; WebMD Today Home WebMD News Center Member Services WebMD University My WebMD Find a Physician Medical Info Check Symptoms Medical Library Quizzes, Calculators Clinical Trials ... Women, Men, Lifestyle Who We Are About WebMD Site Map Health Topics Symptoms ... For a Complete Report Tricho Dento Osseous Syndrome Important It is possible that the main title of the report Tricho Dento Osseous Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report. Synonyms TDO Syndrome Disorder Subdivisions TDO-I TDO-II TDO-III General Discussion Tricho-Dento-Osseous (TDO) syndrome is a rare inherited multisystem disorder that belongs to a group of diseases known as ectodermal dysplasias. Ectodermal dysplasias typically affect the hair, teeth, nails, and/or skin. TDO syndrome is characterized by kinky or curly hair; poorly developed tooth enamel; and unusual thickness and/or denseness (sclerosis) of the top portion of the skull (calvaria) and/or the long bones (i.e., bones in the arms and legs). In some cases, affected individuals also exhibit abnormally thin, brittle nails or premature closure (fusion) of the fibrous joints between certain bones in the skull (craniosynostosis), causing the head to appear abnormally long and narrow (dolicocephaly). There may be three distinct types of TDO syndrome. Some researchers suggest that these variants may be differentiated mainly by whether the calvaria and/or long bones exhibit abnormal hardening (sclerosis), thickening, and/or density. Other symptoms also vary among the three disorder types. TDO syndrome is inherited as an autosomal dominant genetic trait.

18. 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

"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

19. Disease Directory : Musculoskeletal Disorders : Congenital Anomalies : Craniosyn HOME. Sagittal Synostosis (Craniostenosis, Craniosynostosis, dolicocephaly, Scaphocephaly, Sagittal Craniostenosis, Sagittal Craniosynostosis). http://www.diseasedirectory.net/Musculoskeletal_Disorders/Congenital_Anomalies/C

Wednesday, June 02, 2004 Musculoskeletal Disorders Congenital Anomalies Arthrogryposis Clubfoot ... Congenital Anomalies : Craniosynostosis About Craniosynostosis - Childrens Hospital San Diego - About Craniosynostosis - Childrens Hospital San Diego, serving the communities of Chula Vista, National City, El Cajon, Oceanside, El Centro, Rancho Bernardo AllRefer Health - Craniosynostosis (Premature Closure of Sutures) - Craniosynostosis (Premature Closure of Sutures) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs Brynne and Craniosynostosis - Personal experiences of a family and a child born with craniosynstosis. Cleft lip, cleft palate, craniosynostosis, pediatric plastic ... - cleft lip, cleft palate, craniosynostosis, microta, hairy nevus, hemangiomas, children's plastic surgery, cleft lip and cleft palate. Craniosynostosis - annotations For Medical Professionals only, registration required. Craniosynostosis,. Print this article, premature fusion of one or more Craniosynostosis - PO Box 11082, * Chattanooga, TN 37401. 800-, 332-2373. Craniosynostosis. What is Craniosynostosis? There are four types of craniosynostosis:

20. Disease Directory : Sagittal Synostosis (Craniostenosis, Craniosynostosis ... HOME. Sagittal Synostosis (Craniostenosis, Craniosynostosis, dolicocephaly, Scaphocephaly, Sagittal Craniostenosis, Sagittal Craniosynostosis)....... http://www.diseasedirectory.net/detailed/30392.aspx

Wednesday, June 02, 2004 Musculoskeletal Disorders Congenital Anomalies Arthrogryposis Clubfoot ... Craniosynostosis : Sagittal Synostosis (Craniostenosis, Craniosynostosis ... Directory Listing Title: Sagittal Synostosis (Craniostenosis, Craniosynostosis ... Description: HOME. Sagittal Synostosis (Craniostenosis, Craniosynostosis, Dolicocephaly, Scaphocephaly, Sagittal Craniostenosis, Sagittal Craniosynostosis). Date Added: 2/19/2004 4:59:24 PM URL: http://www.bdid.com/sagittal.htm

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