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1. Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome,Intrauterine Dwarfism,
Dubowitz Syndrome,intrauterine dwarfism,Dubowitz Syndrome,IntrauterineDwarfism,Dubowitz Syndrome,intrauterine dwarfism.
http://www.icomm.ca/geneinfo/dubowitz.htm
Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome,Intrauterine Dwarfism
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
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DISORDERS GLOSSARY Dubowitz Syndrome
(as defined by the
National Organization for Rare Disorders

also known as:
Intrauterine Dwarfism

Dubowitz Syndrome is a very rare developmental disorder characterized by growth retardation, short stature, and unusual facial and physical characteristics. Symptoms may develop while the fetus is still in the uterus (intrauterine) or immediately after birth (neonatal). Physical characteristics associated with Dubowitz Syndrome include a high nasal bridge, underdevelopment of the bony ridges above the eyes (supraorbital ridges), widely spaced eyes (ocular hypertelorism), and/or droopy eyelids (ptosis). Affected children typically have patchy areas of itchy red skin (eczema) on their face, knees, and elbows.

2. Dubowitz Syndrome - Quest Diagnostics Patient Health Library
s) and disorder subdivision(s) covered by this report. Synonyms. intrauterine dwarfism. Disorder Subdivisions is still in the uterus (intrauterine) as well as immediately after birth
http://www.questdiagnostics.com/kbase/nord/nord198.htm
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National Organization for Rare Disorders, Inc.
Dubowitz Syndrome
Important
It is possible that the main title of the report 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
  • Intrauterine Dwarfism
Disorder Subdivisions
  • None
General Discussion
Dubowitz syndrome is a very rare genetic and developmental disorder involving multiple congenital (inherited) anomalies including but not limited to: (1) growth failure/short stature; (2) unusual but characteristic facial features; (3) a small head (microencephaly); (4) mild (usually) mental retardation; and (5), in at least 50% of the cases, eczema. Multiple organ systems are affected and the disorder is unpredictable and extremely variable in its expression. Symptoms may be detected while the fetus is still in the uterus (intrauterine) as well as immediately after birth (neonatal).
Facial appearance is a key to the diagnosis, with characteristic high or sloping forehead; sparse hair; flat, undeveloped (hypoplastic) bones above the eyes (supraorbital ridges); increased distance between the eyes (ocular hypertelorism); drooping eyelids (ptosis); sparse (hypoplastic) lateral eyebrows; very small lower jaw (micrognathia) and receding chin (retrognathia). Affected children are often hyperactive, stubborn and shy.

3. Dubowitz Syndrome 1
Dubowitz syndrome 1. Synonym. dwarfismeczema-peculiar facies syndrome A syndrome of intrauterine dwarfism, short stature, mental retardation, sparse hair, eczema, and characteristic
http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome272.html
Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes
View the Full Record
Syndrome Dubowitz syndrome 1 Synonym dwarfism-eczema-peculiar facies syndrome Summary A syndrome of intrauterine dwarfism, short stature, mental retardation, sparse hair, eczema, and characteristic facies. The phenotype varies from normal growth and head circumference with mild psychomotor retardation and lack of eczema to severe growth and mental retardation, microcephaly, behavioral problems, aplastic anemia, immunological disorders, neoplasms, and eczema Some features of this syndrome are similar to those in Bloom and fetal alcohol syndromes. Major Features Head and neck: Microcephaly, micrognathia, prognathism triangular face, high sloping forehead, craniosynostosis, narrow bifrontal diameter, dolichocephaly, trigonocephaly, small face and narrow face, brachycephaly, large open fontanels, prominent occiput, prominent glabella, flat occiput, and Robin sequence. Ears: Large or small ears, low-set posteriorly angulated ears, hypoplastic helices, anteverted auricles, prominent lower anthelices, folded helices, cup-shaped ears, hypoplastic tragus, and ear or pre-auricular fistulae. Otitis media is frequent. Eyes: Blepharophimosis, blepharoptosis, telecanthus, hypertelorism or hypotelorism, upslanted or downslanted palpebral fissures, epicanthus, arched eyebrows, strabismus, esotropia, microphthalmia, iris coloboma, nystagmus, anisocoria, megalocornea, iris hypoplasia, oculomotor paralysis, astigmatism, blue sclera, deep optic nerve cupping, immature retinal vessels, and tortuosity of retinal vessels.

4. EMedicine - Silver-Russell Syndrome : Article By Ainu Prakash-Cheng, MD, PhD
Patients present with intrauterine growth retardation, difficulty feeding, failure to thrive, or A A syndrome of "intrauterine dwarfism" recognisable at birth with craniofacial
http://www.emedicine.com/ped/topic2099.htm
(advertisement) Home Specialties CME PDA ... Patient Education Articles Images CME Patient Education Advanced Search Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease
Silver-Russell Syndrome
Last Updated: December 12, 2003 Rate this Article Email to a Colleague Synonyms and related keywords: SRS, Russell-Silver syndrome, Silver-Russell dwarfism, Silver syndrome AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography
Author: Ainu Prakash-Cheng, MD, PhD , Assistant Professor of Human Genetics and Pediatrics, Department of Human Genetics, Mount Sinai School of Medicine Coauthor(s): Margaret McGovern, MD, PhD , Vice Chair, Associate Professor, Department of Human Genetics, Mount Sinai School of Medicine Ainu Prakash-Cheng, MD, PhD, is a member of the following medical societies: American Academy of Pediatrics American Society of Gene Therapy , and American Society of Human Genetics Editor(s): Elaine H Zackai, MD , Director of Clinical Genetics Center, Professor of Pediatrics, Department of Pediatrics, Division of Human Genetics and Molecular Biology, University of Pennsylvania, Children's Hospital of Philadelphia;

5. Definitions Of Genetic Disorders-I.
htm Intracranial Neoplasm astrocyt.htm Intracranial Tumors braintumr.htm IntracranialVascular Malformations vasmalbrain.htm intrauterine dwarfism dubowitz.htm
http://www.icomm.ca/geneinfo/def-i.htm
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
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DISORDERS GLOSSARY
Definitions of Genetic Disorders beginning with the letter I Click on the link next to the disorder to view its definition. I-Cell Disease icell.htm
Iatrogenic Hypoglycemia hypoglyc.htm
IBGC fahr.htm
IBIDS Syndrome tayich.htm
IBM ibm.htm
IBS ibs.htm
IC interstcyst.htm I-Cell Disease icell.htm ICD spastort.htm ICE Syndrome Cogan-Reese Type cogan.htm Icelandic Type Amyloidosis (Type VI) amylo.htm I-Cell Disease icell.htm Ichthyosiform Erythroderma Corneal Involvement and Deafness kid.htm Ichthyosiform Erythroderma Hair Abnormality Growth and Men tayich.htm Ichthyosiform Erythroderma with Leukocyte Vacuolation chandorf.htm Ichthyosis ichthy.htm Ichthyosis Congenita ichthy.htm Ichthyosis Congenital with Trichothiodystrophy tayich.htm

6. Dubowitz Syndrome
s) covered by this report. Synonyms intrauterine dwarfism. DisorderSubdivisions None. General Discussion Dubowitz syndrome is a very
http://my.webmd.com/hw/health_guide_atoz/nord198.asp
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You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... For a Complete Report Dubowitz Syndrome Important It is possible that the main title of the report Dubowitz 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
  • Intrauterine Dwarfism
Disorder Subdivisions
  • None
General Discussion Dubowitz syndrome is a very rare genetic and developmental disorder involving multiple congenital (inherited) anomalies including but not limited to: (1) growth failure/short stature; (2) unusual but characteristic facial features; (3) a small head (microencephaly); (4) mild (usually) mental retardation; and (5), in at least 50% of the cases, eczema. Multiple organ systems are affected and the disorder is unpredictable and extremely variable in its expression. Symptoms may be detected while the fetus is still in the uterus (intrauterine) as well as immediately after birth (neonatal). Facial appearance is a key to the diagnosis, with characteristic high or sloping forehead; sparse hair; flat, undeveloped (hypoplastic) bones above the eyes (supraorbital ridges); increased distance between the eyes (ocular hypertelorism); drooping eyelids (ptosis); sparse (hypoplastic) lateral eyebrows; very small lower jaw (micrognathia) and receding chin (retrognathia). Affected children are often hyperactive, stubborn and shy.

7. Untitled
intrauterine dwarfism (5) http//directory.google.co.nz/Top/Health/ Conditions_and_Diseases. intrauterine dwarfism intrauterine dwarfism@ (5) http//search.aol.com/cat.adp?id=168 layer
http://www.healthmednet.com/INT-KAN.htm
INT - KAN Int. Cystitis http://health.excite.com/ Int. Cystitis http://www.webcrawler.com/health/diseases_and_conditions/conditions_a_z/conditions_i_l Integrative Medicine http://my.webmd.com/content/healthwise/30/7398 Integrative Medicine [special-topic] http://content.health.msn.com/content/healthwise/106/26476 Intellectual Disabilities http://www.mic.Ki.Se/Diseases/index.html Intensive Care—See Critical Care http://www.vh.org/navigation/vh/topics/adult_patient_index.html Intensive Care see Critical Care http://www.nlm.nih.gov/medlineplus/all_healthtopics.html Intentional weight loss http://health.yahoo.com/encyclopedia/a.html Interace - Marriage / Family [shc] http://content.health.msn.com/content/healthwise/106/26476 Interactive - Johns Hopkins http://www.intelihealth.com/IH/ Intercongregational Alcoholism Program - Addictions [shc] http://content.health.msn.com/content/healthwise/106/26476 Intercongregational Alcoholism Program - Alcohol Abuse [shc] http://content.health.msn.com/content/healthwise/106/26476 Intercostal retractions http://health.yahoo.com/encyclopedia/a.html

8. Index
Intracranial Tumors Intracranial Vascular Malformations Intractable Hiccups IntraepidermalSquamous cell Carcinoma intrauterine dwarfism Intrauterine Synechiae
http://my.webmd.com/hw/index/index-topics-I.asp
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You are in Medical Library Choose a Topic Our Content Sources Ask A Question Clinical Trials Health Guide A-Z Health Topics Symptoms Medical Tests Medications ... Support Organizations Search the Help Health Topics Click a letter to see a list of topics beginning with that letter A B C D ... IV I I Cell Disease back to top IB IBIDS Syndrome IBM IBS (Irritable Bowel Syndrome) back to top IC IC ICD ICE Syndrome, Cogan-Reese Type ICE Syndrome, Essential Iris Atrophy Type ... back to top ID Identifying and avoiding migraine triggers Identifying and avoiding tension headache triggers Identifying asthma triggers Idiopathic Alveolar Hypoventilation ... back to top IG IgA Nephropathy back to top IH IHIS back to top IL Illinois Type Amyloidosis back to top IM Immune Defect due to Absence of Thymus Immune Globulin Immune Hemolytic Anemia Immune Hemolytic Anemia, Paroxysmal Cold ... back to top IN INAD Inborn Error of Urea Synthesis, Arginase Type

9. Online CDR: Medical Term Listing
ACHONDROGENESIS (NEONATAL DWARFISM HYPOCHONDROGENESIS LETHAL OSTEOCHONDRODYSPLAS. ACHONDROPLASIA/ DWARFISM SYNDROME (DJS) DUBOWITZ SYNDROME (intrauterine dwarfism) DUMPING SYNDROME
http://fsnnc.med.unc.edu/Search/medicalTermList.asp
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Local FSNs Services ... About Us Online CDR Medical/Disability Term s Below is a listing of medical/disability terms used in our database. 11;22 TRANSLOCATION (PARTIAL TRISOMY 11;22)
11Q SYNDROME (JACOBSEN SYNDROME, DELETION ON LONG ARM OF CHROMOSOME 11)
18P- SYNDROME (18 P MINUS, SHORT ARM 18 DELETION, CHROMOSOME 18, MONOSOMY 18P)
18Q- SYNDROME (18 Q MINUS, CHROMOSOME 18 LONG ARM DELETION)
4Q- SYNDROME (4 Q MINUS)
8P DUPLICATION (CHROMOSOME 8P DISORDER)
AARSKOG SYNDROME
ABDOMINAL MIGRAINE
ABDOMINAL PAIN
ABSENCE OF FINGERS - CONGENITAL (COMPLETE OR PARTIAL) ACADEMICALLY GIFTED/TALENTED ACHALASIA ACHONDROGENESIS (NEONATAL DWARFISM,HYPOCHONDROGENESIS,LETHAL OSTEOCHONDRODYSPLAS ACHONDROPLASIA/ DWARFISM ACHROMATOPSIA (ROD MONOCHROMACY, BLUE CONE MONOCHROMACY)

10. Dubowitz Syndrome
covered by this report. Synonyms. intrauterine dwarfism. Disorder Subdivisions.None. Related Disorders List. Information on the following
http://www.bchealthguide.org/kbase/nord/nord198.htm
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National Organization for Rare Disorders, Inc.
Dubowitz Syndrome
Important
It is possible that the main title of the report 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
  • Intrauterine Dwarfism
Disorder Subdivisions
  • None
Related Disorders List
Information on the following diseases can be found in the Related Disorders section of this report:
  • Bloom Syndrome Seckel Syndrome Fetal Alcohol Syndrome (FAS) Ectodermal Dysplasias
General Discussion
Dubowitz syndrome is a very rare genetic and developmental disorder involving multiple congenital (inherited) anomalies including but not limited to: (1) growth failure/short stature; (2) unusual but characteristic facial features; (3) a small head (microencephaly); (4) mild (usually) mental retardation; and (5), in at least 50% of the cases, eczema. Multiple organ systems are affected and the disorder is unpredictable and extremely variable in its expression. Symptoms may be detected while the fetus is still in the uterus (intrauterine) as well as immediately after birth (neonatal).
Facial appearance is a key to the diagnosis, with characteristic high or sloping forehead; sparse hair; flat, undeveloped (hypoplastic) bones above the eyes (supraorbital ridges); increased distance between the eyes (ocular hypertelorism); drooping eyelids (ptosis); sparse (hypoplastic) lateral eyebrows; very small lower jaw (micrognathia) and receding chin (retrognathia). Affected children are often hyperactive, stubborn and shy.

11. Koo Koo - The Bird Girl
and was afflicted with "birdheaded dwarfism", also called Seckel's syndrome, nanocephaly, or syndrome is a form of intrauterine dwarfism (symptoms present before birth) that
http://phreeque.tripod.com/koo-koo.html
Minnie Woolsey a.k.a. Koo Koo, the Blind Girl from Mars, was born in 1880 and was afflicted with "bird-headed dwarfism", also called Seckel's syndrome, nanocephaly, or Harper's syndrome. Other individuals with nanocephaly included Caroline Crachami, the "Sicilian Fairy" (1815-1824) and Nicholas Ferry (1741-1764), the king of Poland's court dwarf. Seckel's syndrome is a form of intrauterine dwarfism (symptoms present before birth) that causes proportional short stature, beak-like nose and large ears, absence of hair and teeth, mental retardation, and joint and limb defects such as clubfoot. Koo Koo, additionally, was blind, and her act included staring into space, not responding to anything around her. Koo Koo appears in Freaks in the brief but memorable scene in which she dances on the table before the wedding feast. I don't know when Koo Koo died, but according to some accounts, she was still alive in 1960, making her at least 80 years old. "I knew Koo-Koo, the Bird Girl. She was a tiny woman with a round body and skinny legs and a gigantic nose like a beak. She actually did look like a bird. But her elevator didn't go all the way to the top floor, you know?" - Melvin Burkhart Betty Green >>

12. Health Topics - Quest Diagnostics Patient Health Library
Intrauterine device (IUD) for birth control. intrauterine dwarfism. Intrauterinefetal blood transfusion for Rh disease. Intrauterine Synechiae. Intussusception.
http://www.questdiagnostics.com/kbase/list/ht/i.htm
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B C D ... I Cell Disease IB
IBIDS Syndrome IBM IBS (Irritable Bowel Syndrome) IC IC ICD ICE Syndrome, Cogan-Reese Type ICE Syndrome, Essential Iris Atrophy Type ... Icterus Intermittens Juvenalis ID Identifying and avoiding migraine triggers Identifying and avoiding tension headache triggers Identifying asthma triggers IDET ... IDPA IG IgA Nephropathy IH IHIS IL Ileoanal or ileorectal anastomosis for ulcerative colitis Illinois Type Amyloidosis IM Top Immune Defect due to Absence of Thymus Immune Globulin Immune Hemolytic Anemia ... Impotent Neutrophil Syndrome IN In vitro fertilization for infertility Inability to Walk, Age 11 and Younger INAD Inborn Error of Urea Synthesis, Arginase Type ... Inverted Smile And Occult Neuropathic Bladder IO Iowa Type Amyloidosis (Type IV) IP IP Top IPA IR IRDS Irideremia Iridocorneal Endothelial (ICE) Syndrome, Cogan-Resse Type Iridocorneal Endothelial (ICE) Syndrome, Essential Iris Atrophy ... Irritable Bowel Syndrome (IBS) IS Isaacs' Syndrome Isaacs-Merten Syndrome Ischemic Necrosis of Bone Islet cell cancer: Treatment - Health Professional Information [Cancer.gov]

13. I
Intracranial Hypotension. intrauterine dwarfism. Iritis. Irritable Bowel Syndrome Hypotension. intrauterine dwarfism. Iritis. Irritable Bowel SyndromeChats and Forums, Research
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    14. Disease Directory : Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome ..
    Diseases Genetic Disorders Dubowitz Syndrome Dubowitz Syndrome,IntrauterineDwarfism,Dubowitz Syndrome Directory Listing.
    http://www.diseasedirectory.net/detailed/25994.aspx
    Wednesday, June 02, 2004 Genetic Disorders
    Aarskog Syndrome

    Aase Syndrome

    Ablepharon-Macrostomia Syndrome
    ... Dubowitz Syndrome : Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome ...
    Directory Listing
    Title: Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome ...
    Description: Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome,Intrauterine Dwarfism,Dubowitz Syndrome,Intrauterine Dwarfism. Dubowitz Syndrome
    Date Added: 2/17/2004 10:09:17 AM
    URL: http://www.icomm.ca/geneinfo/dubowitz.htm

    15. NORD - National Organization For Rare Disorders, Inc.
    Synonyms of Dubowitz Syndrome. intrauterine dwarfism. Disorder Subdivisions detected while the fetus is still in the uterus (intrauterine) as well as immediately after birth (neonatal
    http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Dubowitz Synd

    16. Disease Directory : Genetic Disorders : Dubowitz Syndrome
    It; Dubowitz Syndrome Support Site Dubowitz Syndrome Support Homepage Linkimage. Dubowitz Syndrome,intrauterine dwarfism,Dubowitz Syndrome
    http://www.diseasedirectory.net/Genetic_Disorders/Dubowitz_Syndrome/default.aspx
    Wednesday, June 02, 2004 Genetic Disorders
    Aarskog Syndrome

    Aase Syndrome

    Ablepharon-Macrostomia Syndrome
    ... Genetic Disorders : Dubowitz Syndrome
    • Conditions and Diseases - Dubowitz Syndrome Top Links - Dubowitz Syndrome Web Site Links. National Library of Medicine - Dubowitz syndrome, a look at the synonyms, a summary and list of major features. Costello Kids - Official site of the International Costello Syndrome Support Group. Includes medical information, photographs and videos, therapy ideas, news, and links. Dubowitz (syndrome de) - Dubowitz (syndrome de). voir ©galement croissance, microc©phalie, r©trognatisme, hypert©lorisme. Affection h©r©ditaire   transmission dubowitz syndrome - 41: dubowitz syndrome. My son has dubowitz syndrome. Re: dubowitz syndrome flamingo 14:27:03 09/10/03 (0): Post A Follow-Up Message! To Dubowitz Syndrome - Dubowitz syndrome is a very rare genetic and developmental disorder involving multiple congenital (inherited) anomalies including but not limited to: (1 Dubowitz Syndrome - Founded 1997. Information, education, support and networking for parents of children with Dubowitz syndrome, and concerned professionals. Dubowitz Syndrome.

    17. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/I
    Intracranial Hypotension@ (1); intrauterine dwarfism@ (4); Iritis@ (19); IrritableBowel Syndrome@ (67); Isaacs Syndrome@ (3). News about I More news about I .
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    18. Swiss Society Of Neonatology
    A syndrome of intrauterine dwarfism recognisable at birth with craniofacial dysostosis,disproportionately short arms and other abnormalities (5 examples).
    http://www.neonet.ch/cotm/html/body_case-june03.html
    A newborn girl with suspected Silver-Russell syndrome
    Nordmann Y, Fauchère JC, Bucher HU
    Clinic of Neonatology, University Hospital Zurich, Switzerland We present the case of a girl with suspected Silver-Russell syndrome (SRS). SRS is a rare, clinically and genetically heterogeneous disorder involving intra-uterine and post-natal growth retardation with a wide spectrum of additional dysmorphic features. Because of the clinical heterogeneity, diagnosis can be rather subjective and is not always easy to confirm. Case presentation
    The girl, third child of a 30-years-old mother, was born prematurely at 31 6/7 weeks of gestation by caesarean section because of a pathologic CTG. Intrauterine growth retardation had been diagnosed at 26 6/7 weeks of gestation. At that time, amniocentesis and TORCH serologies were performed with inconspicuous results.
    Fig. 1. Large appearing head, high forehead, downturning corners of the mouth. Fig. 2. Asymmetry of the legs. Fig. 3. Weight and height Fig. 4.

    19. Iritis
    Interstitial Cystitis@ (23) Intracranial Hypotension@ (2) intrauterine dwarfism@(4) Iritis@ (19) Irritable Bowel Syndrome@ (67) Isaacs Syndrome@ (3 ..
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