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         Intrauterine Dwarfism:     more detail

21. Health, Conditions And Diseases, Genetic Disorders: Dubowitz Syndrome
A syndrome of intrauterine dwarfism, short stature, mental retardation,sparse hair, eczema, and characteristic facies. The phenotype
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Related links of interest: 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. Help build the largest human-edited directory on the web.

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Explosive Disorder (12) Internet Addiction (26), Interstitial Cystitis (21) IntestinalFlu (9) Intracranial Hypotension (1) intrauterine dwarfism (4) Iritis (19
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23. Health/Conditions And Diseases/I
Disorder@ 12 Internet Addiction@ 26 Interstitial Cystitis@ 21 Intestinal Flu@11 Intracranial Hypotension@ 1 intrauterine dwarfism@ 4 Iritis@ 19
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24. Health, Conditions And Diseases, I
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  • 25. Delv.co.uk: Internet Addiction Websites In The UK
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    26. Index - A To Z Âå¾Ç¹Ï®ÑÀ] - °ê»Ú«p¥Í°·±d¶é°Ï - 24Drs.com
    Intraepidermal Squamous cell Carcinoma nord Intrauterine device (IUD) for birthcontrol surgicaldetail intrauterine dwarfism nord Intrauterine Synechiae
    http://www.24drs.com/Health_Guide/health.asp?who=4115.21644

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    28. Principles Of Pediatric Dermatology - Chapter 32 : GENODERMATOSES
    The hair may be sparse and prematurely gray. Diagnosis. The syndrome mustbe differentiated from others in which there is intrauterine dwarfism.
    http://www.drmhijazy.com/english/chapters/chapter32_2.htm
    CHAPTER 32 GENODERMATOSES Contents Search
    Recessive epidermolysis bullosa
    The recessive dystrophic epidermolysis bullosa has the same cutaneous features of the dominant type. Skin manifestations Large, flaccid often-hemorrhagic bullae appear after birth or early in infancy. Mucous membrane manifestations Severe scarring of the mucous membranes of the mouth, pharynx, esophagus and the condition may be fatal. Nail dystrophy is a common complication of the recessive type of epidermolysis bullosa. Secondary bacterial infection is common and causes more complications.
    Fig. 256. Epidermolysis, Recessive
    Dystrophic Type
    Fig. 257. Epidermolysis Bullosa
    Differential Diagnosis
  • Bullous diseases
    In infancy, differentiation of epidermolysis bullosa from other bullous eruptions is rarely a problem. Benign chronic bullous disease of childhood may mimic inverse types of EB since the blistering occurs around the genitalia, perineum and buttocks. However, histology of these conditions is diagnostic and the presence of linear IgA on direct immunofluorescence may help to confirm the diagnosis. Dominant bullous ichthyosiform erythroderma.
  • 29. Anales Españoles De Pediatría: Texto Completo: Enanismo Intrauterino Y Rasgos
    Translate this page Disomía uniparental del cromosoma 7. Retraso del crecimiento fetal. Nanismo intrauterino.Recién nacido. intrauterine dwarfism and dysmorfic features.
    http://db.doyma.es/cgi-bin/wdbcgi.exe/doyma/mrevista.fulltext?pident=13013413

    30. Healthcyclopedia Index - I
    Intermittent Explosive Disorder, Interstitial Cystitis. Intracranial Hypotension,intrauterine dwarfism. Iritis, Irritable Bowel Syndrome. Isaacs Syndrome,
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    31. LookSmart - Directory - Conditions And Illnesses I
    Disease; Intestinal Obstruction. IntraAbdominal Abscess; IntracranialHypotension; intrauterine dwarfism; Inverted Nipple; Iritis; Iron
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    32. J Med Genet -- MONK Et Al. 38 (4): 11
    2. Russell A. A syndrome of intrauterine dwarfism recognised at birth with craniofacialdysostosis, disproportionate short arms and other anomalies.
    http://www.jmedgenet.com/cgi/content/full/38/4/e11

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    J Med Genet e11 ( April )
    Electronic letters
    No evidence for mosaicism in Silver-Russell syndrome
    E DITOR Silver-Russell syndrome (SRS) is a condition characterised by pre- and postnatal growth restriction, triangular facies, and limb and truncal asymmetry. The aetiology of the syndrome is heterogeneous and there is no clearly established Mendelian basis. A number of chromosomal abnormalities are associated with the SRS phenotype in a minority of cases. To date, 37 cases of maternal uniparental disomy for chromosome 7 (mUPD(7)) have been reported, representing approximately 10% of all cases. Five mUPD(7) probands were found to show heterodisomy for the complete length of chromosome 7, ruling out the exposure of a mutant recessive gene as the basis of SRS.

    33. J Med Genet -- KOSAKI Et Al. 37 (9): 19
    1. Russell A. A syndrome of intrauterine dwarfism recognizable at birth withcraniofacial dysostosis, disproportionate short arms and other anomalies.
    http://www.jmedgenet.com/cgi/content/full/37/9/e19

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    J Med Genet e19 ( September )
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    Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assay
    E DITOR In approximately 10% of patients with Silver-Russell syndrome, pre- and postnatal growth retardation with relative macrocephaly, triangular facies, and asymmetry is associated with maternal uniparental disomy of chromosome 7 (UPD(7)mat). The purpose of this report is to present a novel assay to diagnose UPD(7)mat by analysing the methylation status of PEG1/MEST , the only known imprinted gene on chromosome 7, which encodes a protein with sequence homology to alpha/ beta-hydrolase. Like its mouse homologue Peg1/Mest the human PEG1/MEST gene is expressed from the paternal allele but not from the maternal allele.

    34. Pre- And Postnatal Growth Retardationsevere Mental Retardation
    keratinized nails. Another example of a distinct syndrome of inheritedintrauterine dwarfism? Cartwright J, Nelson M, Fryns JP. Department
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    35. I In Health > Conditions And Diseases
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    36. J Med Genet -- WAKELING Et Al. 37 (1): 65
    2. Russell A. A syndrome of intrauterine dwarfism recognizable at birth withcraniofacial dysostosis, disproportionate short arms and other anomalies.
    http://jmg.bmjjournals.com/cgi/content/full/37/1/65

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    J Med Genet 65-67 ( January )
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    Biallelic expression of and , two candidate genes for the Silver-Russell syndrome
    E DITOR Silver-Russell syndrome (SRS) is a condition characterised by intrauterine and postnatal growth retardation with relative sparing of cranial growth, triangular facies, fifth finger clinodactyly, and facial, limb, or truncal asymmetry. The molecular basis of SRS remains elusive and seems likely to be heterogeneous. However, maternal uniparental disomy of chromosome 7 (mUPD7) has been found in approximately 10% of SRS patients, suggesting that at least one gene on chromosome 7 is imprinted and involved in the pathogenesis of this condition.

    37. Fablis Directory For /Health/Conditions_and_Diseases/I
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    38. Lukol Directory - Health Conditions And Diseases I
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