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61. Cybershaman Session Specific Diseases/Disorders Sale
Blister. blochsulzberger syndrome ( see Incontinentia Pigmenti). bloch-sulzberger syndrome ( see Incontinentia Pigmenti). Blood Coagulation Disorders.
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62. Syndromes Rares Associés Au Strabisme (Bosnjakovska 1997)
Translate this page Summary Incontinentia pigmenti (bloch-sulzberger syndrome) is a very rare syndrome characterized by damage of the nuroectodermal and muscle-skeletal tissues.
http://orthoptie.net/jfo/jfo29/bosnjako97.htm
SYNDROMES RARES ASSOCIÉS AU STRABISME
(Incontinentia pigmenti et Arthrogryposis congénitale) S. BOSNJAKOVSKA, N. POP-JORDANOVA
(Skopje - Macédoine) Résumé : Incontinentia pigmenti (syndrome de Bloch-Sulzberger) est une maladie très rare, caractérisée par des affections du tissu neuroectodermal oculaire et musculo-squelettique. Environ 95% des cas sont observés chez les patients du sexe féminin. Nous rapportons ici un cas extrêmement rare chez un garçon.Outre les altérations cutanées manifestées dès le deuxième jour de la naissance, on a découvert ultérieurement une atrophie du nerf optique de l'oeil gauche ainsi qu'un strabisme du même oeil. A l'âge de six ans, l'enfant présentait des anomalies orthodontiques : absence de cinq dents de lait et de onze dents définitives.
Arthrogrypose congénitale est aussi un syndrome rare, caractérisé par la contracture des articulations et des troubles hétérogènes vastes. Nous présentons ici le cas d'une fille âgée de 10 ans. En dehors des troubles principaux, elle manifeste aussi un strabisme, un nystagmus, une amblyopie et un ptôsis. Mots clés : Incontinentia pigmenti, atrophie optique, strabisme, anomalies orthodontiques, arthrogrypose, ptôsis

63. Incontinentia Pigmenti
Google, WWW Medical.WebEnds.com. Incontinentia Pigmenti. blochsulzberger syndrome; Bloch Sulzberger Syndrome; Syndrome, Bloch-Sulzberger.
http://medical.webends.com/kw/Incontinentia Pigmenti
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Incontinentia Pigmenti
Bloch-Sulzberger Syndrome; Bloch Sulzberger Syndrome; Syndrome, Bloch-Sulzberger A genodermatosis occurring mostly in females and characterized by skin changes in three phases - vesiculobullous, verrucous papillomatous, and macular melanodermic. Hyperpigmentation is bizarre and irregular. Sixty percent of patients have abnormalities of eyes, teeth, central nervous system , and skin appendages.
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64. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/B
Birthmarks@ (5); Bites and Stings@ (30); Blastomycosis@ (4); Blepharospasm@ (10); Blindness@ (94); blochsulzberger syndrome@ (7); Blood
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65. GREENSEEK
symptoms. » National Library of Medicine bloch-sulzberger syndrome, the synonyms, a summary and major features. » Readers Digest
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66. B In Health > Conditions And Diseases
Birthmarks@ (10); Bites and Stings@ (30); Blastomycosis@ (7); Blepharospasm@ (10); Blindness@ (104); blochsulzberger syndrome@ (7); Blood
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67. 2095: Skewed X-inactivation In Incontinentia Pigmenti (IP2).
Incontinentia Pigmenti (IP2) or blochsulzberger syndrome is a rare neurocutaneous syndrome characterized by developmental abnormalities of the tissues and
http://www.faseb.org/genetics/ashg99/f2095.htm
Program Nr: 2095 Skewed X-inactivation in Incontinentia Pigmenti (IP2). A. Smahi, S. Heuertz, J.P. Bonnefont, A. Delanay, P. Vabres, A. Munnich. Genetique INSERM U393, Hopital Necker, Paris, France.

68. NORD - National Organization For Rare Disorders, Inc.
BlochSiemens-Sulzberger Syndrome; bloch-sulzberger syndrome; IP; Pigmented Dermatosis, Siemens-Bloch type. Disorder Subdivisions General
http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Incontinentia

69. Cytogenetics Publications
Pal K, Handyside A, Braude P Ogilvie CM (2000) A pregnancy following PGD for Xlinked autosomal dominant incontinentia pigmenti (bloch-sulzberger syndrome).
http://www.kcl.ac.uk/depsta/memoge/cytogeneticspublications.html
Cytogenetics
Mackie Ogilvie C (2003) Prenatal diagnosis for chromosome abnormalities: past, present and future. Pathol Biol Paris, 51, 156-160. Mackie Ogilvie C (2003) Preimplantation genetic diagnosis. (Letter) Lancet, 362 (9379) 250. Ogilvie CM (2003) Uses of error: laboratory diagnosis. Lancet, 361 (9352) 160. Mackie Ogilvie C & Scriven PN (2001) The scope and limitations of "FISH" for preimplantation genetic diagnosis. (Letter) Fertil Steril, 75, 227-228. Ogilvie CM, Phil D & Scriven PN (2001) The scope and limitations of "FISH" for preimplantation genetic diagnosis. Fertil Steril 75, 227-228.
Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. Am J Med Genet, 96 (2) 228-234.
Scriven PN (1998) Communicating chromosome rearrangements and their outcomes using simple computer-generated color ideograms. Genet Test 2, 71-74.
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71. Incontinentia Pigmenti (Bloch-Sulzberger) Syndrome
Incontinentia Pigmenti (blochsulzberger) syndrome Fact Sheet in Ukrainian by IBIS
http://www.ibis-birthdefects.org/start/ukrainian/ublokh.htm

Ïðî I.B.I.S.

Ïðèºäíàéòåñü äî I.B.I.S.

Witkop Incontinentia pigmenti; IP.
  • Gorlin RJ, Cohen MM Jr, Hennekam RCM. Syndromes of the Head and Neck. Fourth Edition. Oxford University Press. 2001:551-554. Jones KL. Smith’s Recognizable Patterns of Human Malformation. 5th Edition. W.B. Saunders Company. 1997:502-503. Warkany J. Congenital Malformations: Notes and Comments. Year Book Medical Publishers, Inc. Part 2. 1991:1171-1173.

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    72. AllRefer Health - Incontinentia Pigmenti Syndrome Complications (Bloch-Sulzberge
    Incontinentia Pigmenti syndrome (blochsulzberger's Disease) information center covers Complications. Alternate Names bloch-sulzberger's Disease. See all Pictures Images
    http://www.1uphealth.com/health/incontinentia_pigmenti_syndrome_complications.ht
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    You are here : AllRefer.com Health Incontinentia Pigmenti Syndrome : Complications of Incontinentia Pigmenti Syndrome
    Incontinentia Pigmenti Syndrome
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    Alternate Names : Bloch-Sulzberger's Disease Complications
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    Complications Calling Your Health Care Provider Topics that might be of interest to you Cataract Mental Retardation Strabismus Other Topics Central Nervous System Genetic Counseling and Prenatal Diagnosis Genetics Hair Loss ... Walking/Gait Abnormalities Review Date : 10/27/2003 Main Page of Incontinentia Pigmenti Syndrome From Our Sponsors: A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's

    73. AllRefer Health - Incontinentia Pigmenti Syndrome (Bloch-Sulzberger's Disease)
    Incontinentia Pigmenti syndrome (blochsulzberger's Disease) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, tests, support groups,
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    Incontinentia Pigmenti Syndrome
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    Alternate Names : Bloch-Sulzberger's Disease Definition Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation.
    Incontinentia Pigmenti on the Leg
    Incontinentia Pigmenti on the Leg Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear.

    74. GASNet Anesthesiology: Bloch - Sulzberger Syndrome
    Bloch Sulzberger syndrome - symptoms and caveats
    http://www.gasnet.org/pediatric-syndromes/bloch-sulzberger.php

    75. AllRefer Health - Incontinentia Pigmenti Syndrome (Bloch-Sulzberger's Disease)
    Alternate Names blochsulzberger s Disease. Definition. Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin
    http://health.allrefer.com/health/incontinentia-pigmenti-syndrome-info.html
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    You are here : AllRefer.com Health Incontinentia Pigmenti Syndrome
    Incontinentia Pigmenti Syndrome
    Definition Prevention
    Treatment

    Expectations or Prognosis
    ...
    Go To Main Page
    Alternate Names : Bloch-Sulzberger's Disease Definition Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation.
    Incontinentia Pigmenti on the Leg
    Incontinentia Pigmenti on the Leg Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear.

    76. AllRefer Health - Incontinentia Pigmenti Syndrome Prevention (Bloch-Sulzberger's
    Incontinentia Pigmenti syndrome. Alternate Names blochsulzberger s Disease. See all Pictures Images Prevention. Genetic counseling
    http://health.allrefer.com/health/incontinentia-pigmenti-syndrome-prevention.htm
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    Incontinentia Pigmenti Syndrome
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    Alternate Names : Bloch-Sulzberger's Disease Prevention Genetic counseling may be of value for prospective parents with a family history of IPS.
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    77. ► Incontinentia Pigmenti Syndrome
    blochsulzberger s disease. Causes, incidence, and risk factors Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait.
    http://www.umm.edu/ency/article/001583.htm
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    Incontinentia pigmenti syndrome
    Overview Symptoms Treatment Prevention Definition: An inherited disorder that causes unusual blistering of the skin followed by increased pigmentation.
    Alternative Names: Bloch-Sulzberger's disease
    Causes, incidence, and risk factors: Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation.
    Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear.
    Most people with IPS also have other problems including abnormal teeth, hair loss , and central nervous system (CNS) abnormalities. CNS problems may include retardation and delayed development

    78. Bl : On Medical Dictionary Online
    Blinds Blink Reflex Blink Reflexes Blinking Blister Blister, Fever Blisters Blisters, Fever Bloat Guard Blocadren Bloch Sulzberger syndrome blochsulzberger
    http://www.online-medical-dictionary.org/?q=~Bl

    79. Congenital, Hereditary, And Neonatal Diseases And Abnormalities
    Incontinentia Pigmenti (blochsulzberger/Siemens syndrome) CH Chang - eMedicine. The US Nat l Incontinentia Pigmenti Foundation - New York.
    http://www.mic.ki.se/Diseases/C16.html
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    Diseases and Disorders Links pertaining to Congenital, Hereditary, and Neonatal Diseases and Abnormalities Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Abnormalities Aicardi Syndrome (not on MeSH) Amniotic Band Syndrome Anencephaly ... Wolf-Hirschhorn Syndrome (not on MeSH)
    Congenital, Hereditary, and Neonatal Diseases and Abnormalities The US National Organization for Rare Disorders , including a Rare Disease Database , and a List of Disease-specific Organizations Search Jablonski's MCA/MR Syndromes Database [Congenital Abnormalities associated with Mental Retardation] - NLM (US) Indice delle malattie [in Italian] - InformaGene (IT) A Short History of Mapping [P Murphy] GENATLAS: Pathology Search [J Frezal] - Univ Rene Descartes, Paris (FR) OrphaNet [rare diseases] - (FR) A Birth Disorder Information Directory - Spamgid.com

    80. Untitled
    Translate this page Synonyme maladie ou syndrome de bloch-sulzberger, dermatose pigmentaire en éclaboussures de Franceschetti et Jadassohn, naevus chromatophore héréditaire
    http://www.vulgaris-medical.net/texti/incontin_pigment.htm
    Incontinentia pigmenti (de Bruno Bloch et Sulzberger)
    En anglais incontinentia pigmenti.
    Synonyme : maladie ou syndrome de Bloch-Sulzberger, dermatose pigmentaire en éclaboussures de Franceschetti et Jadassohn, naevus chromatophore héréditaire de Naegeli, mélanose dégénérative du chorion de Siemens.
    Affection touchant essentiellement le sexe féminin dont plus de 95 % des cas. Il s' agit d'une dermatose (maladie de peau) dont l'origine est le plus souvent congénitale et héréditaire, touchant les petites filles et évoluant en plusieurs phases :
    Tout d'abord une phase pendant laquelle l'enfant présente des bulles au niveau des membres, parfois sur le reste du tronc. Cette phase qui dure quelques semaines à quelques mois est suivie de l'apparition de lésions de type verruqueux sur les mains et les pieds et entre l'âge de 2 à 5 mois.
    La phase suivante se caractérise par la survenue d'une pigmentation (coloration de la peau) couleur chocolat sous forme de taches, de bandes, de plaques ou en bandes. Cette dermatose prend caractéristiquement la forme d'éclaboussures ou niveau du tronc. Cette troisième phase s'atténue ensuite au moment de l'adolescence et est parfois la seule de la maladie.
    Le problème de cette pathologie ne réside pas dans la survenue de dermatoses mais dans celle de malformations qu'il est nécessaire de rechercher. Il s' agit avant tout d'une atteinte dentaire (des dents) et oculaire (des yeux dans 30 % des cas). Ces anomalies sont avant tout un strabisme, une atteinte du globe oculaire, une cataracte est parfois une cécité (le patient devient aveugle).

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