61. CONGENITAL ANOMALIES 743.0 anophthalmos. 743.00 Clinical anophthalmos, unspecified Agenesis Congenitalabsence of eye anophthalmos NOS 743.03 Cystic eyeball, congenital http://www.thera.info/icd9-cm/sect-740-759.html

CONGENITAL ANOMALIES (740-759) Anencephalus and similar anomalies Spina bifida Other congenital anomalies of nervous system Congenital anomalies of eye ... Other and unspecified congenital anomalies 740 Anencephalus and similar anomalies 740.0 Anencephalus Acrania Amyelencephalus Hemianencephaly Hemicephaly 740.1 Craniorachischisis 740.2 Iniencephaly 741 Spina bifida Excludes: spina bifida occulta (756.17) The following fifth-digit subclassification is for use with category 741: unspecified region 1 cervical region 2 dorsal (thoracic) region 3 lumbar region 741.0 With hydrocephalus Arnold-Chiari syndrome, type II Chiari malformation, type II Any condition classifiable to 741.9 with any condition classifiable to 742.3 741.9 Without mention of hydrocephalus Hydromeningocele (spinal) Hydromyelocele Meningocele (spinal) Meningomyelocele Myelocele Myelocystocele Rachischisis Spina bifida (aperta) Syringomyelocele 742 Other congenital anomalies of nervous system 742.0 Encephalocele Encephalocystocele Encephalomyelocele Hydroencephalocele Hydromeningocele, cranial

62. ICD-9-CM From Code 740 743.0 anophthalmos. 743.00 Clinical anophthalmos, unspecified. Agenesis;Congenital absence of eye; anophthalmos NOS. 743.03 Cystic eyeball, congenital http://www.dmi.columbia.edu/hripcsak/icd9/1tabular740.html

CONGENITAL ANOMALIES (740-759) 740 Anencephalus and similar anomalies 740.0 Anencephalus Acrania Amyelencephalus Hemianencephaly Hemicephaly 740.1 Craniorachischisis 740.2 Iniencephaly 741 Spina bifida Excludes: spina bifida occulta (756.17) The following fifth-digit subclassification is for use with category 741: 0 unspecified region 1 cervical region 2 dorsal (thoracic) region 3 lumbar region 741.0 With hydrocephalus Arnold-Chiari syndrome, type II Chiari malformation, type II Any condition classifiable to 741.9 with any condition classifiable to 742.3 741.9 Without mention of hydrocephalus Hydromeningocele (spinal) Hydromyelocele Meningocele (spinal) Meningomyelocele Myelocele Myelocystocele Rachischisis Spina bifida (aperta) Syringomyelocele 742 Other congenital anomalies of nervous system 742.0 Encephalocele Encephalocystocele Encephalomyelocele Hydroencephalocele Hydromeningocele, cranial Meningocele, cerebral Meningoencephalocele 742.1 Microcephalus Hydromicrocephaly Micrencephaly 742.2 Reduction deformities of brain Absence of part of brain Agenesis of part of brain Agyria Aplasia of part of brain Arhinencephaly Holoprosencephaly Hypoplasia of part of brain Microgyria 742.3 Congenital hydrocephalus

63. Clinical Trial: Molecular Analysis Of Microphthalmia/Anophthalmia Sensi A, Incorvaia C, Sebastiani A, Calzolari E. Clinical anophthalmos in a family.Clin Genet. 1987 Sep;32(3)1569. http://www.clinicaltrials.gov/show/NCT00011843

Home Search Browse Resources ... About Molecular Analysis of Microphthalmia/Anophthalmia This study is currently recruiting patients. Verified by National Institutes of Health Clinical Center (CC) February 2, 2005 Sponsored by: National Human Genome Research Institute (NHGRI) Information provided by: National Institutes of Health Clinical Center (CC) ClinicalTrials.gov Identifier: Purpose This study will try to learn more about the genetic cause and symptoms of microphthalmia (small eyes) or anophthalmia (absence of one or both eyes). Patients with microphthalmia or anophthalmia with mental retardation may be eligible for this study. Patients' parents and siblings will also be included for genetic studies. Patients may participate in both the clinical and laboratory parts of the study or just the laboratory part, as described below: Laboratory The laboratory study consists of DNA analysis to determine the genetic cause of microphthalmia/anophthalmia. The DNA sample is obtained using one of the following methods: -Blood draw - for young children, a numbing cream is applied to the skin before the needlestick to decrease the pain

64. Portal Toolkit Invalid Site URL Congenital clinical anophthalmos. Newborn girl with bilateral congenital clinical Therapy for anophthalmos with enlarging conformers, and results. http://www.co-ophthalmology.com/pt/re/coophth/fulltext.00055735-200410000-00008.

Sorry, the URL specified, http://www.co-ophthalmology.com:80/pt/re/coophth/fulltext.00055735-200410000-00008.htm , is invalid. To go to site for "TEST-Current Opinion in Ophthalmology" please click here http://www.co-ophthalmology.com To go to site for "Current Opinion in Ophthalmology" please click here http://www.co-ophthalmology.com To go to the LWW Online site, please click here http://www.lwwonline.com Thank you

65. NSW Health - ICD-9-CM 740-759 743.00 Clinical anophthalmos, unspecified Agenesis Congenital absence of eyeanophthalmos NOS 743.03 Cystic eyeball, congenital 743.06 Cryptophthalmos http://www.health.nsw.gov.au/public-health/icd/740-759.htm

14. CONGENITAL ANOMALIES (740-759) 740 Anencephalus and similar anomalies Anencephalus Acrania Amyelencephalus Hemianencephaly Hemicephaly Craniorachischisis Iniencephaly 741 Spina bifida Excludes : spina bifida occulta (756.17) The following fifth-digit subclassification is for use with category 741: unspecified region 1 cervical region 2 dorsal (thoracic) region 3 lumbar region With hydrocephalus Arnold-Chiari syndrome, type II Chiari malformation, type II Any condition classifiable to 741.9 with any condition classifiable to 742.3 Without mention of hydrocephalus Hydromeningocele (spinal) Hydromyelocele Meningocele (spinal) Meningomyelocele Myelocele Myelocystocele Rachischisis Spina bifida (aperta) Syringomyelocele 742 Other congenital anomalies of nervous system Encephalocele Encephalocystocele Encephalomyelocele Hydroencephalocele Hydromeningocele, cranial Meningocele, cerebral Meningoencephalocele

66. Oculoplastic Surgery - Reconstructive Surgery - VisionChannel A child born without an eyeball (congenital anophthalmos) usually has a small eye Cosmetic procedures for children with congenital anophthalmos are http://www.visionchannel.net/oculoplasticsurgery/reconstructive.shtml

Home Search SiteMap Ask the Dr. ... Medical Store OCULOPLASTIC SURGERY Overview Cosmetic Surgery Corrective Surgery Repair of Eyelid Malpositions Reconstructive Surgery Orbital Decompression Enucleation Implantation CONDITIONS Amblyopia (lazy eye) Blepharitis Cataracts Color Vision Deficiency ... Refractive Errors Correction Retinal Detachment Retinitis Pigmentosa Retinopathy of Prematurity Skin Cancer of the Eyelids Tear Duct Obstruction RESOURCES Anatomy Basic Eye Exam Clinical Trials Glossary ... What Is an Ophthalmologist? What Is an Optometrist? What Is an Optician? Videos ABOUT US Healthcommunities.com Pressroom Testimonials Bibliography Reconstructive Surgery Surgical removal of skin cancer of the eyelid is standard therapy. Depending on the size, depth, and location of the lesion, this can cause substantial loss of eyelid skin that may affect its function and appearance. Surgeons attempt to preserve as much skin as possible and minimize scarring, while making sure that all of the cancer cells are removed. Moh’s technique, (link) or frozen section control, for example, enables the surgeon to excise the tumor while leaving more healthy tissue intact. Some very small tumors may heal on their own, through a process called granulation A large tumor may require reconstructive surgery. Two methods used are

67. The EyePathologist Disease - A anophthalmos X-linked - Klintworth, Gordon K. anophthalmos with associatedanomalies - Klintworth, Gordon K. Anterior ischemic optic neuropathy http://www.eyepathologist.com/List.asp

To see an alphabetized list of diseases illustrated and described in the EyePathologist database click the appropriate initial letter. You must Register to view the entire EyePathologist program, which includes sections on Anatomy and Pathology as well as an interactive Glossary of over 5,000 terms. A B C D E ... Z Aarskog syndrome - Klintworth, Gordon K. Aarskog-Scott syndrome - Klintworth, Gordon K. Abetalipoproteinemia - Elliott, Alexandra; Florakis, George J.; Vrabec, Michael P. Abetalipoproteinemia - classic - Elliott, Alexandra; Florakis, George J.; Vrabec, Michael P. Abetalipoproteinemia - normotriglyceridemic - Elliott, Alexandra; Florakis, George J.; Vrabec, Michael P. Abiotrophic ophthalmoplegia externa - Engle, Elizabeth C. Ablepharia - Klintworth, Gordon K. Ablepharon - Klintworth, Gordon K. Abscess - vitreous - Klintworth, Gordon K. Acanthamebiasis - Klintworth, Gordon K. Acanthamoeba infection - Klintworth, Gordon K. Acanthoma - Klintworth, Gordon K. Acanthoma - clear cell - Klintworth, Gordon K.

68. EUROCAT anophthalmos/micropthalmos, , 7430, 7431, Q110, Q111, Q112. anophthalmos,Unilateral or bilateral absence of the eye tissue. 7430, Q110, Q111 http://www.biomedicalweb.biz/eurocat/appendices.cgi

Coding Of Anomalies: Anomaly Description Of Anomaly Comments Nervous system Nervous system anomalies include neural tube defects, hydrocephaly, microcephaly and other anomalies of the brain, spinal cord and nervous system Neural Tube Defects Neural tube defects include anencephaly, encephalocele, spina bifida and iniencephacy Anencephalus and similar Absence or deficience of a major portion of the cranial vault, the covering skin and the brain tissue. (incompatible with life) Encephalocele Herniation of the brain and/or meninges through a defect in the skull exclude if associated with anencephalus Spina Bifida Midline defect of the osseous spine ususally affecting the posterior arches resulting in a herniation or exposure of the spinal cord and/or meninges exclude if associated with anencephalus, or encephalocele Hydrocephaly Dilation of ventricular system, not due to primary atrophy of the brain, with or without enlargement of the skull 7423, excl 74232 exclude hydranencephaly, or association with NTDs Microcephaly Reduction in the size of the brain with a skull circumference less than three standard deviations below the mean for gestation or age and reduced growth during first year of life exclude association with NTDs Arhinencephaly/holoprosencephaly Absence of the first cranial (olfactory) nerve tract. There is a spectrum of anomalies from a normal brain, except for the first cranial nerve tract, to a single ventricle (holoprosencephaly)

69. Araceli Busby EUROCAT.ulst.ac.uk/pdf/CaptureRecapture.pdf; Busby A, Dolk H, Armstrong BGanophthalmos/microphthalmos in England temporal variation and the association http://www.lshtm.ac.uk/pehru/staff/abusby.html

Contact People Sitemap A-Z ... Departments You are here: Home Departments PHP PEHRU ... Staff Araceli Busby BSc RGN MSC PhD Title: Research Fellow Disciplines: Epidemiology. Research areas: Perinatal health, Reproductive health, Environment. Other keywords: congenital anomalies. Room: 40A Keppel Street Telephone: Fax: Email: a.busby@lshtm.ac.uk Background Teaching Research Selected publications Carolyn Stephens, Rupert Hough, Araceli Busby. (March 2004). Assessing the health risk and impact associated with living on the Thames View Estate. A rapid literature review of methods. Report for Barking and Dagenham PCT. www.barkinghaveringhealth.nhs.uk/pdfs/tvriskassess.pdf Lenore Abramsky, Nicola Armstrong, Araceli Busby, Helen Dolk and a EUROCAT Working Group. Prevention of Neural Tube Defects by Periconceptional Folic Acid Supplementation in Europe. EUROCAT Special Report, May 2003. http://www.EUROCAT.ulst.ac.uk/pubdata/folic%20acid.html Armstrong B, Busby A, Dolk H. Using capture recapture methods to ascertain completeness of a register: case study and methodological considerations. EUROCAT Special Report, November 2003. http://www.EUROCAT.ulst.ac.uk/pdf/Capture-Recapture.pdf

70. MEANWHILE BACK IN IRAQ AND VIETNAM I have not seen any reports on anophthalmos cases (babies born without eyes)associated with these compounds, but this data may well be in company files. http://www.firethistime.org/meanwhileiniraq.htm

MEANWHILE....BACK IN IRAQ (and Vietnam) "The Security Council began to streamline its vetting procedures in March 2000, when the total value of blocked contracts stood at about 1.7 billion dollars. In his letter, Sevan said a total of 1,854 contracts were now on hold, worth a total 4.956 billion dollars. They included orders for 4.28 billion dollars worth of humanitarian supplies and for 676 million dollars worth of oil industry equipment." - from 'UN alarmed by contract blocking of Iraq oil-for-food programme,' reported by Agence France Press, 9th January 2002 "In 30 years in Washington I've never seen anything quite like it. They're being treated like enemies because of a policy disagreement." - Richard Perle, US Defense Policy Board Chairman and reiterated by former CIA Director James Woolsey, quoted in the Wall Street Journal, 10th January 2002 Perle was describing the US State Deptartment decision to suspend funding to the INC citing financial irregularities. The INC (Iraqi National Congress - in opposition to Saddam Hussein) had been pledged $97 million and were given a January 15th 2002 deadline to produce accounts. The State Department announcement came 10 days ahead of schedule. The INC informed them that undercover sources in Iraq would be compromised by full disclosure. A CHAMBER OF HORRORS NEXT TO THE GARDEN OF EDEN by Andy Kershaw The Independent 1st December 2001 I thought I had a strong stomach - toughened by the minefields and foul frontline hospitals of Angola, by the handiwork of the death squads in Haiti and by the wholesale butchery of Rwanda. But I nearly lost my breakfast last week at the Basrah Maternity and Children's Hospital in southern Iraq.

71. Publications - Childhood Eye Diseases variation in blindness in children due to microphthalmos, anophthalmos andcoloboma. and pedigrees in children with anophthalmos in southern India. http://www.iceh.org.uk/res_pu03.asp

Search ICEH I Contact us I Site directory Current Research I Research Publications I Cochrane Eyes and Vision Group Research Publications ICEH research publication lists, organised by topic: Blindness I Cataract I Childhood Eye Diseases I Cornea I Glaucoma I Onchocerciasis I Refractive errors I Retina and Optic Nerve diseases I Trachoma I Others Childhood Eye Diseases Books and Chapters Papers: 2000 onwards I I Books and Chapters Gilbert CE. Prevention of childhood blindness. In: Fielder A, Best A, Bas M, eds. Clinics in Developmental Medicine: Management of Visual Impairment in Childhood. UK: Mac Keith Press, 1993: 180-208. Foster A, Gilbert CE. Epidemiology of visual impairment in children. In: Taylor D, ed. Paediatric Ophthalmology (2nd Edition). Oxford: Blackwell, 1997: 3-12. Foster A, Gilbert C. Childhood Blindness. In: Strategies for the Prevention of Blindness in National Programmes. 2nd Edition. World Health Organization, Geneva, 1997 McLaren DS.

72. BIRTH DEFECTS (BD) RATES IN UKRAINE(1) (2001 - 2000) IBIS Total anophthalmos / Microphthalmos (include unspecified) (2), 4, 1, nr, 2.02,NA. anophthalmos (2), 0, 0, nr, 0.00, NA http://ibis-birthdefects.org/start/ubdrate3.htm

Tips for printing BIRTH DEFECTS (BD) RATES IN UKRAINE About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Music Prodigies Data for 2001 (Rivne and Volyn oblasts) Live births (L) Stillbirths (S) Total births Number of terminations of pregnancy (ToP) for birth defects (1) (nr) Birth Defects Number of cases Rates * 10000 Livebirths Stillbirths ToP* L+S L+S+ToP Anencephaly N.A. Spina bifida N.A. Encephalocele N.A. Microcephaly (2) nr N.A. Arhinencephaly / Holoprosencephaly nr N.A. Hydrocephaly nr N.A. Total Anophthalmos / Microphthalmos (include unspecified) (2) nr N.A. Anophthalmos (2) nr N.A. Microphthalmos (2) nr N.A. Total Anotia / Microtia (include unspecified) nr N.A. Anotia nr N.A. Microtia nr N.A. Transposition of great vessels nr N.A. Tetralogy of Fallot nr N.A. Hypoplastic left heart syndrome nr N.A. Coarctation of aorta nr N.A. Choanal atresia, bilateral nr N.A. Cleft palate without cleft lip nr N.A. Cleft lip with or without cleft palate nr N.A.

73. BIRTH DEFECTS (BD) RATES IN UKRAINE(1) (2001 - 2000) IBIS Total anophthalmos / Microphthalmos (include unspecified) (2), 5, 0, nr, 1.92,NA. anophthalmos (2), 1, 0, nr, 0.38, NA http://ibis-birthdefects.org/start/ukbdrate.htm

Tips for printing BIRTH DEFECTS (BD) RATES IN UKRAINE About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Music Prodigies Data for 2000 (Rivne and Volyn oblasts) Live births (L) Stillbirths (S) Total births Number of terminations of pregnancy (ToP) for birth defects (1) Birth Defects Number of cases Rates * 10000 Livebirths Stillbirths ToP* L+S L+S+ToP Anencephaly N.A. Spina bifida N.A. Encephalocele N.A. Microcephaly (2) nr N.A. Arhinencephaly / Holoprosencephaly nr N.A. Hydrocephaly nr N.A. Total Anophthalmos / Microphthalmos (include unspecified) (2) nr N.A. Anophthalmos (2) nr N.A. Microphthalmos (2) nr N.A. Total Anotia / Microtia (include unspecified) nr N.A. Anotia nr N.A. Microtia nr N.A. Transposition of great vessels nr N.A. Tetralogy of Fallot nr N.A. Hypoplastic left heart syndrome nr N.A. Coarctation of aorta nr N.A. Choanal atresia, bilateral nr N.A. Cleft palate without cleft lip nr N.A. Cleft lip with or without cleft palate nr N.A.

74. Lenz Microphthalmia Syndrome Synonyms. Lenz Syndrome; Lenz Dysplasia; Microphthalmia or anophthalmos withAssociated Anomalies (obsolete); MAA; Lenz Dysmorphogenetic Syndrome http://www.bchealthguide.org/kbase/nord/nord1057.htm

var hwPrint=1;var hwDocHWID="nord1057";var hwDocTitle="Lenz Microphthalmia Syndrome";var hwRank="1";var hwSectionHWID="nord1057-Header";var hwSource="en-caQ2_05";var hwDocType="Nord"; National Organization for Rare Disorders, Inc. Lenz Microphthalmia Syndrome Important It is possible that the main title of the report Lenz Microphthalmia 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 Lenz Syndrome Lenz Dysplasia Microphthalmia or Anophthalmos with Associated Anomalies (obsolete) MAA Lenz Dysmorphogenetic Syndrome Disorder Subdivisions None General Discussion Lenz Microphthalmia syndrome is an extremely rare inherited disorder characterized by abnormal smallness of one or both eyes (unilateral or bilateral microphthalmos) and/or droopy eyelids (blepharoptosis), resulting in visual impairment. In rare cases, affected infants may exhibit complete absence of the eyes (anophthalmia). Most affected infants also exhibit developmental delay and mental retardation, ranging from mild to severe. Additional physical abnormalities are often associated with this disorder such as an unusually small head (microcephaly) and/or malformations of the teeth, ears, and/or fingers and/or toes (digits). The range and severity of findings may vary from case to case. Lenz microphthalmia syndrome, which is inherited as an X-linked recessive genetic trait, is fully expressed in males only. However, females who carry one copy of the disease gene (heterozygotes) may exhibit some of the symptoms associated with the disorder, such as an abnormally small head (microcephaly), short stature, and/or malformations of the fingers and/or toes.

75. GeneCard For ANOP1 anophthalmos 1 (with mental retardation, without limb anomalies or dental orurogenital abnormalities) Symbol approved by the HUGO Gene Nomenclature http://www.genecards.org/cgi-bin/carddisp?ANOP1

76. Adbusters : "A Culture Of Life" In babies born in Iraq in 2002, the incidence of anophthalmos was 250000 times .. . the natural occurrence.” The White House s dodging and weaving to duck http://adbusters.org/blogs/A_Culture_of_Life.html

Recent Posts virgin The Art Fart Survey Something Rotten in Denmark The Excuse Makers: Condoleezza Rice ... What is RSS? "A Culture of Life" April 5, 2005 Specimen room at Tu Du hospital, Ho Chi Minh City. From the book Agent Orange: "Collateral Damage" in Viet Nam , Philip Jones Griffiths. “A nation that has already suffered 20 years of warfare will suffer once again. Armies on both sides will take new casualties. And the war will go on.” So said US president Lyndon Johnson in March 1968 of the war in Vietnam. History would prove him supremely correct. By the time it was over, America’s longest-running military engagement—90 months of bloody guerilla warfare—would kill 58,000 Americans and 1.5 million Vietnamese. But for some 4 million more Vietnamese citizens—those exposed to the toxic herbicide Agent Orange—the war is still being fought today. Used by the United States to kill the thick foliage that hid enemy troops, Agent Orange contains the most dangerous form of dioxin, TCDD. US planes sprayed 11 million gallons of it between 1962 and 1971, dispersing what has been called the “most toxic molecule on earth” throughout a country Johnson aimed to make “free of any outside domination or interference.” Ever since, US veterans and Vietnamese citizens have suffered a horrifying array of health problems linked to Agent Orange, from miscarriages to severe birth defects in their offspring, cancer to diabetes. But, while the US government and Agent Orange’s manufacturers have agreed to compensate US veterans for suffering caused by exposure to the herbicide, no such justice has been found for Vietnam’s victims.

77. UNSW Embryology-OMIM Syndactyly List *309800 MICROPHTHALMIA OR anophthalmos, WITH ASSOCIATED ANOMALIES; MAA *309801MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS 122920 CRANIOFRONTAL DYSPLASIA http://embryology.med.unsw.edu.au/OMIMfind/skmus/OMIM-syndactyly_list.htm

UNSW Embryology MUSCULOSKELETAL DEVELOPMENT Embryology Home Page Select Entries from OMIM Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Internet access computers can see the full description of the abnormality from the links below. Back to UNSW Embryology-Musculoskeletal Notes 169 entries found, searching for " syndactyly SYNDACTYLY, TYPE III SYNDACTYLY, TYPE IV SYNDACTYLY, TYPE V CRYPTOPHTHALMOS WITH OTHER MALFORMATIONS SYNDACTYLY, TYPE I SYNDACTYLY, TYPE II ECTODERMAL DYSPLASIA, CLEFT LIP AND PALATE, HAND AND FOOT DEFORMITY, AND MENTAL RETARDATION SYNDACTYLY, TYPE I, WITH MICROCEPHALY AND MENTAL RETARDATION CENANI SYNDACTYLISM SCLEROSTEOSIS SAETHRE-CHOTZEN SYNDROME; SCS SYNDACTYLY WITH RENAL AND ANOGENITAL MALFORMATIONS ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY ANOPHTHALMOS WITH LIMB ANOMALIES POLAND SYNDROME SYNDACTYLY-POLYDACTYLY-EARLOBE SYNDROME LONG QT SYNDROME WITH SYNDACTYLY APHALANGIA, PARTIAL, WITH SYNDACTYLY AND DUPLICATION OF METATARSAL IV

78. Information Center For Rare Diseases And Orphan Drugs anophthalmos anophthalmos clinical anophthalmos with limb anomalies anorectalanomalies anotia anotia facial palsy cardiac defect http://www.raredis.org/modules/sections/index.php?op=printpage&artid=25

79. All India Ophthalmological Society - India's Biggest Ophthalmic Organisation Treatment of anophthalmos and Socket reconstruction. Smith B, Obear M, LeoneCR Jr. The correction of anophthalmos associated with anophthalmos by glass http://www.aios.org/proceedings.cfm?pid=390&show=y

80. Link Directory - Finnish Information Center On Mental Retardation anophthalmos, TRUE OR PRIMARY, OMIM anophthalmos, eMedical Journal anophthalmos,Geometry Sourcebook covering anophthalmos, ICON Health Publications http://www.saunalahti.fi/kup/engl/webs_g.html

Finnish Information Center on Mental Retardation English links A B C D ... Z G deletion Syndrome (monosomy 22) chromosome 22 monosomy syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance, Pinto-Escalante D et al, Am J Med Genet. 1998 - PubMed A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome JL Watt et al, Journal of Medical Genetics, 1985 Full mosaic monosomy 22 in a child with DiGeorge syndrome facial appearance, Doris Pinto-Escalante et al, Wiley InterScience 1999 ... Alagillen oireyhtymä; monosomia 20p12 Galloway-Mowat Syndrome Galloway Mowat Syndrome, NORD Galloway syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes MICROCEPHALY, HIATUS HERNIA, AND NEPHROTIC SYNDROME, OMIM, Victor A. McKusick Pachygyria and congenital nephrosis disorder of migration and neuronal orientation, Robain O, Deonna T, Acta Neuropathol (Berl). 1983 - PubMed ... Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome, Garty BZ, Eisenstein B, Sandbank J, Kaffe S, Dagan R, Gadoth N, J Med Genet. 1994 - PubMed Gamma-aminobutyrate transaminase 4-@AMINOBUTYRATE AMINOTRANSFERASE; ABAT, OMIM

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