21. The Sudroid (Indo-African) Race dolicocephaly ( longheadedness ) is common amongst Sudras. dolicocephaly iscommon amongst East Africans in general ( Nilotes, Sudanic Blacks and 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 -

22. 22q13 dolicocephaly This means having a long skull with prominent forehead dolicocephaly Having a long head, or a skull that is longer than it is broad. 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.

23. The Aryans Came Down Like Wolves On The Flock dolicocephaly dolicocephaly ( long-headedness ) is common amongst Sudras. Infact, many are classed as hyperdolicocephalic. dolicocephaly http://www.hindu-religion.net/printthread.php?Board=hinduism&main=37439&type=pos

24. Anophthalmia - Megalocornea - Cardiopathy - Skeletal Anomalies The child had several other anomalies musche hypoplasia, growth retardation,dolicocephaly, skull asymmetry with right occipital and left supraorbital http://www.orpha.net/static/GB/anophthalmia__megalocornea__cardiopathy__skeletal

Orphanet database access Anophthalmia - megalocornea - cardiopathy - skeletal anomalies Direct access to data Summary Clinical signs Abnormal corneal structure Aniridia Autosomal recessive inheritance Megalocornea Microphthalmos Blepharophimosis/short palp. fissures Congenital cardiac anomaly Dolicho/Scaphocephaly Ear anomaly (shape/structure) High vaulted/narrow palate Inguinal hernia Long philtrum Midface anomalies Mitral valve prolapse/incompetence Night blindness/hemeralopia Optic disc anomaly/atrophy Pectus excavatum Plagiocephaly Prognathism Pupillary anomalies Scoliosis Tricuspid valve prolapse/incompetence Umbilical hernia Update : 04/09/2005 Orphanet database access

25. CHROMOSOME 22 CENTRAL dolicocephaly; lymphedema; mild dilitation of cerebral ventricles mild facial dysmorphic features; dolicocephaly; downslanting palpebral fisuures http://www.nt.net/~a815/22q13.htm

SUPPORT FOR CHROMOSOME 22 RELATED DISORDERS Click here for an online membership form to JOIN US! Registered members receive our newsletter and can choose to be listed in our parent registry. Also, join our discussion list What would you like to do? I want to learn about chromosome 22 disorders I want to find out about current news I want to learn about current research I want to connect with other families ... on other genetic disorders I want to return to the main index We are proud members of the Genetic Alliance. Volunteers, professional input and donations are welcomed NOTE FROM 22q13 FOUNDATION REGARDING NAME.... 22q13 DELETION SYNDROME NOW HAS 2ND NAME: PHELAN-McDERMID SYNDROME Nick Assendelft Vice-President 22q13 Deletion Syndrome Foundation Phelan-McDermid Syndrome Editor, Deletion 22q13 UPDATE Vice-Chair, Communications Committee

26. Chromosome 22 Central dolicocephaly (don’t know) lymphedema (don’t know) mild dilation of cerebralventricles (Dane has) dysplastic ears (low set, large ears may have) http://www.nt.net/~a815/dane.htm

SUPPORT FOR CHROMOSOME 22 RELATED DISORDERS Click here for an online membership form to JOIN US! Registered members receive our newsletter and can choose to be listed in our parent registry. Also, join our discussion list What would you like to do? I want to learn about chromosome 22 disorders I want to find out about current news I want to learn about current research I want to connect with other families ... on other genetic disorders I want to return to the main index We are proud members of the Genetic Alliance. Volunteers, professional input and donations are welcomed Stories listed by disorder category: 22q11 deletion (VCFS, DiGeorge) Emanuel Syndrome - partial trisomy 11/22 Mosaic Trisomy 22 Ring 22 22q13 deletion ... Unique Disorders Would you like to share your story? Fill in our story submission form to be included on this website. We hope you enjoy reading about our special children! Dane Basher DOB: 7/23/99 22q13 Deletion Parents Cynthia Dulaney and Cern Basher Cincinnati, Ohio

27. Support Groups Sagittal Synostosis Sagittal Synostosis Homepage Sagittal synostosis (also known as scaphocephaly,dolicocephaly, sagittal craniostenosis, or sagittal craniosynostosis), 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

28. Kenyaniyetu - Are Kenyans That Ugly??!!! Wantangazaji walifikiri amevaa kofia! jina scientific la chogo kama la huyo mkenyani dolicocephaly waNilotes wa kenya ndiyo wana michogo kama hiyo. http://kenyaniyetu.com/v20/forums/printthread.php?s=4a8b35d038fed7140a2f34868932

29. Sagittal Synostosis Also known as scaphocephaly or dolicocephaly, the sagittal suture closes earlyand restricts groth of the head in the side to side direction. http://cpmcnet.columbia.edu/dept/nsg/PNS/cf/sagittal.html

Also known as scaphocephaly or dolicocephaly , the sagittal suture closes early and restricts groth of the head in the side to side direction. This forces the head to grow in a front to back direction which leads to a narrow elongated head. Usually there is an associated fullness or "bossing" to the forehead.

30. CCDD: References: Links: Craniosynostosis Conditions Scaphocephaly. Sagittal Synostosis Homepage, Scaphocephaly, dolicocephaly, sagittalcraniostenosis, or sagittal craniosynostosis. scaphocephaly, http://www.hopkinsmedicine.org/craniofacial/References/LinkList.cfm?Category=All

31. CCDD: Family: References: Links: Craniosynostosis Conditions Sagittal Synostosis Homepage, Scaphocephaly, dolicocephaly, sagittal craniostenosis,or sagittal craniosynostosis. scaphocephaly, premature closure of http://www.hopkinsmedicine.org/craniofacial/References/LinkList.cfm?Category=Fam

32. Health Library - fusion) of the fibrous joints between certain bones in the skull (craniosynostosis),causing the head to appear abnormally long and narrow (dolicocephaly). http://hvelink.saint-lukes.org/library/healthguide/IllnessConditions/topic.asp?h

33. Program Nr 855 Patient 1 is an 18 year old severely mentally impaired male with dolicocephaly,high arched palate, flat nasal bridge, acquired total alopecia, prominent ears http://www.faseb.org/genetics/ashg00/f855.htm

Program Nr: 855 Deletion of 2q37 and duplication of 10q24: Report of two cases in the same family and literature review. A. Wiktor , G.L. Feldman , E. Bawle , P. Czarnecki , J. Conard , D.L. Van Dyke 1) Department of Medical Genetics, Henry Ford Health System, Detroit, MI; 2) Division of Genetic and Metabolic Disorders, Children's Hospital of Michigan, Detroit, MI; 3) Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI.

34. Program Nr 95 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

Program Nr: 95 Deletion 22q13 syndrome - under-recognized and under-diagnosed. M.C. Phelan , R.C. Rogers , D.B. Everman , G.A. Stapleton , N.R. Powers , S.R. Shaw 1) T C Thompson Children's Hosp, Chattanooga, TN; 2) Greenwood Genetic Center, Greenwood, SC; 3) The Children's Hospital, Greenville, SC.

35. The Chromosome 7 Annotation Project Karyotype, 46, XY, der(14)t(7;14)(p11;p11) mat, Phenotype, dolicocephaly, widefontanelle, hypertelorism, antimongoloid slanting of the palpebral fissures http://www.chr7.org/edit_clinical.php?browser=gbrowse&uniqueid=699358_proband&br

36. The Chromosome 7 Annotation Project Karyotype, 46, XX, der(14)t(7;14)(p11;p11) , Phenotype, dolicocephaly, hypertelorism,craniopalaoskisis, dysmorphic hands, hypoplasia of the labia majora http://www.chr7.org/edit_clinical.php?browser=gbrowse&uniqueid=2080099&breaktype

37. Article : Fetal Choroid Plexus Cysts - A Practical Approach In The Perspective O atresia Hydronephrosis Club foot deformity Clenched hands Generalised arthogryposisMicrognathia Microphthalmos Hypertelorism dolicocephaly Prominent occiput http://www.journal-obgyn-india.com/articles/issue_july_august2001/o_paper_82.asp

Current Issue Editorial Obstetric Papers Gynec Papers ... Gynec Cases J Obstet Gynecol Ind Vol.51, No. 4: July/August 2001 Pg 82-84 OBSTETRIC PAPERS Fetal Choroid Plexus Cysts : A Practical Approach in the Perspective of Available Data Kuldeep Singh, Ashok Khurana The Ultrasound Lab, C 584 Defence Colony, New Delhi 110 024. Summary Introduction Material and Methods Table I Sonographic Stigmata ofTrisomy 18 Polyhydramnios Intra-uterine growth retardation Congenital heart disease Diaphragmatic hernia Omphalocele Esophageal atresia Hydronephrosis Club foot deformity Clenched hands Generalised arthogryposis Micrognathia Microphthalmos Hypertelorism Dolicocephaly Prominent occiput Posterior cranial fossa abnormalities Agenesis of corpus callosum Single umbilical artery Thickened nuchal translucency Observation and Results Fig.1. Unilateral large choroid plexus cyst in a 19 week fetus.

38. Netscape Search Category - D Disorders @ (775); Diptheria @ (4); Dissociative Identity Disorder @ (114);Diverticulitis @ (26); dolicocephaly @ (3); Down Syndrome @ (58 http://207.200.81.7/Health/Conditions_and_Diseases/D

Autos Browser Central Computing Entertainment Games Health International Lifestyles Local Guide Music News Personal Finance Shopping Small Business Sports Travel Weather Home Health Conditions and Diseases D Business Games Health News Recreation Reference Regional Shopping Sports World Specialized Searches Yellow Pages White Pages MapQuest Maps Product Search ... Job Search Learn More Search directly from your browser. Internet Keywords Affiliate Program Frequent Questions Tips on Searching Get Involved Help build the largest human-edited directory on the web. Become an Editor Suggest a Site Get the latest Communicator. Search the Web or Ask a Question Search the entire directory Search only in D Deafblindness Deafness Dementia Dengue Fever ... Dysphagia Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Last update: 11:22:53 GMT, Saturday, March 10, 2001 Help Site Map Advertise with Us Add Site ... Terms of Service

39. Cyber Café > Vieux Port > Marseille > France > Europe > Planete Developmental Delay@ (14); Diabetes@ (261); Diabetes Insipidus@ (18); DiabeticRetinopathy@ (8); dolicocephaly@ (3); Down Syndrome@ (69 http://info-cafe.fr/repertoires.php?/Bookmarks/A/aseaguy69/Diseases_A_to_Z/

40. Entry Page Observations included dolicocephaly, malar hypoplasia, low set, posteriorly rotatedears, ptosis, downslanting palpebral fissures, and microretrognathia. http://fenice.tigem.it/srs6bin/cgi-bin/wgetz?-id 4xSuY1LlhLN [omim-ID:182212] -e

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