Hypomelanosis of Ito and Related Disorders (Pigmentary Mosaicism)

[1]  P. Sharma,et al.  Nevus depigmentosus affecting the iris and skin: a case report , 2008, Journal of the European Academy of Dermatology and Venereology : JEADV.

[2]  H. Kang,et al.  Partial unilateral lentiginosis colocalized with naevus depigmentosus , 2008, Clinical and experimental dermatology.

[3]  G. Ghiggeri,et al.  Glomerulocystic kidney disease in hypomelanosis of Ito , 2008, Pediatric Nephrology.

[4]  H. Shen,et al.  Clinical, histopathological and ultrastructural characteristics of naevus depigmentosus , 2008, Clinical and experimental dermatology.

[5]  G. Spadola,et al.  Lentigines within Nevus Depigmentosus: A Rare Collateral Effect of UVB Therapy? , 2008, Pediatric dermatology.

[6]  M. Gönül,et al.  Pediatric Skin Disorders Encountered in a Dermatology Outpatient Clinic in Turkey , 2008, Pediatric dermatology.

[7]  Do Young Kim,et al.  Recurrence of nevus depigmentosus after an autologous epidermal graft. , 2008, Journal of the American Academy of Dermatology.

[8]  Won-Soo Lee,et al.  Linear and whorled nevoid hypermelanosis: unique clinical presentations and their possible association with chromosomal abnormality inv(9). , 2008, Archives of dermatology.

[9]  S. Aktaş,et al.  Becker's naevus and segmental naevus depigmentosus: An example of twin spotting? , 2007, The Australasian journal of dermatology.

[10]  V. Lernia.  Linear and Whorled Hypermelanosis , 2007 .

[11]  H. Hong,et al.  A birthmark survey in 500 newborns: clinical observation in two northern Taiwan medical center nurseries. , 2007, Chang Gung medical journal.

[12]  R. Raju,et al.  The Clinical Profile of Children in India with Pigmentary Anomalies along the Lines of Blaschko and Central Nervous System Manifestations , 2007, Pediatric dermatology.

[13]  Eun-So Lee,et al.  Clinical and histopathologic characteristics of nevus depigmentosus. , 2006, Journal of the American Academy of Dermatology.

[14]  S. Bondanza,et al.  Autologous in vitro reconstituted epidermis in the treatment of a large nevus depigmentosus. , 2006, Journal of the American Academy of Dermatology.

[15]  R. Happle.  X-chromosome inactivation: role in skin disease expression. , 2006, Acta paediatrica (Oslo, Norway : 1992). Supplement.

[16]  S. Khandpur,et al.  Systematized nevus depigmentosus. , 2005, Indian pediatrics.

[17]  C. Adamsbaum,et al.  Hypomelanosis of Ito and brain abnormalities: MRI findings and literature review , 1996, Pediatric Radiology.

[18]  T. Moritani,et al.  Hypomelanosis of lto associated with neuroblastoma , 2005, Pediatric Radiology.

[19]  Y. Maeoka,et al.  Hypomelanosis of ito: MR findings , 2005, Pediatric Radiology.

[20]  J. Weinreb,et al.  Unusual brain MRI findings in a patient with Hypomelanosis of Ito , 2005, Pediatric Radiology.

[21]  R. Happle.  [Patterns on the skin. New aspects of their embryologic and genetic causes]. , 2004, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

[22]  N. Riyaz,et al.  Hemihypertrophy and primary small intestinal lymphangiectasia in incontinentia pigmenti achromians. , 2004, Indian journal of pediatrics.

[23]  D. Bennett,et al.  Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes , 2004, The British journal of dermatology.

[24]  K. Sardana,et al.  Colocalized nevus depigmentosus and lentigines with underlying breast hypoplasia: a case of reverse mutation? , 2004, Dermatology online journal.

[25]  T. H. Newton,et al.  The rare phakomatoses. , 2004, Neuroimaging clinics of North America.

[26]  R. Pagon,et al.  Hypomelanosis of Ito in a girl with plexus papilloma and transloction (X;17) , 1994, Human Genetics.

[27]  C. Lacroix,et al.  Central nervous system lesions in hypomclanosis of Ito: an MRI and pathological study , 1993, Journal of Neurology.

[28]  G. Utermann,et al.  Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17) , 1993, Human Genetics.

[29]  G. Casara,et al.  Hypomelanosis of Ito and hemimegalencephaly , 1990, Child's Nervous System.

[30]  C. Turleau,et al.  Hypomelanosis of Ito (incontinentia pigmenti achromians) and mosaicism for a microdeletion of 15q1 , 1986, Human Genetics.

[31]  Y. Liao,et al.  Coexistence of congenital linear punctate keratoderma and nevus depigmentosus with lentigines: a case of twin spotting? , 2004, Acta dermato-venereologica.

[32]  R. Happle.  Lyonization and the lines of Blaschko , 2004, Human Genetics.

[33]  M. Bobrow,et al.  Two cases of X/autosome translocation in females with incontinentia pigmenti , 2004, Human Genetics.

[34]  E. Grosshans,et al.  Incontinentia pigmenti achromians (ITO) Étude ultrastructurale , 2004, Archiv für klinische und experimentelle Dermatologie.

[35]  WenChieh Chen,et al.  Black lunula caused by Tegafur. , 2004, Acta dermato-venereologica.

[36]  M. Ruggieri,et al.  Delineation of a newly recognized neurocutaneous malformation syndrome with “cutis tricolor” , 2003, American journal of medical genetics. Part A.

[37]  J. Utikal,et al.  Nevi flammei affecting two contralateral quadrants and nevus depigmentosus: A new type of phacomatosis pigmentovascularis? , 2003, American journal of medical genetics. Part A.

[38]  D. Horn,et al.  Pigmentary mosaicism of the hyperpigmented type in two half-brothers. , 2002, American journal of medical genetics.

[39]  R. Happle,et al.  Segmental lentiginosis with ipsilateral nevus depigmentosus: another example of twin spotting? , 2002, European journal of dermatology : EJD.

[40]  K. Song,et al.  Development of multiple pigmented nevi within segmental nevus depigmentosus. , 2002, Journal of Korean medical science.

[41]  V. Lernia.  Segmental nevus depigmentosus: Analysis of 20 patients , 2002 .

[42]  A. Polizzi,et al.  Tumors and hypomelanosis of Ito. , 2009, Archives of pathology & laboratory medicine.

[43]  Sharon E. Albers,et al.  Textbook of Pediatric Dermatology , 2001 .

[44]  R. Happle.  Phylloide Hypomelanose und Mosaiktrisomie 13 Ein neues ätiologisch definiertes neurokutanes Syndrom , 2001, Der Hautarzt.

[45]  M. Ruggieri.  Familial hypomelanosis of ito: implications for genetic counselling. , 2000, American journal of medical genetics.

[46]  M. Ruggieri,et al.  Topical Review: Hypomelanosis of Ito: Clinical Syndrome or Just Phenotype? , 2000, Journal of child neurology.

[47]  M. Ruggieri.  Cutis tricolor: congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: further expansion of the phenotype , 2000, European Journal of Pediatrics.

[48]  L. Juhlin,et al.  Unilateral lentiginosis with nevus depigmentosus on the other side. , 2000, Journal of the American Academy of Dermatology.

[49]  S. Klauck,et al.  Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti , 2000, Nature.

[50]  A. König,et al.  Hypomelanosis of Ito: no entity, but a cutaneous sign of mosaicism. , 1999, American journal of medical genetics.

[51]  C. Moss.  Cytogenetic and molecular evidence for cutaneous mosaicism: the ectodermal origin of Blaschko lines. , 1999, American journal of medical genetics.

[52]  Effendy.  Mosaicism in human skin , 1999, American journal of medical genetics.

[53]  H. Rehder,et al.  Pigmentary mosaicism in hypomelanosis of Ito , 1998, Human Genetics.

[54]  R. Happle.  Incontinentia pigmenti versus hypomelanosis of Ito: the whys and wherefores of a confusing issue. , 1998, American journal of medical genetics.

[55]  J. Ogunbiyi,et al.  Nevus depigmentosus and inflammatory linear epidermal nevus – an unusual combination with a note on histology , 1998, International journal of dermatology.

[56]  S. Pascual-Pascual,et al.  Hypomelanosis of ITO. A study of 76 infantile cases , 1998, Brain and Development.

[57]  R. Happle.  A rule concerning the segmental manifestation of autosomal dominant skin disorders. Review of clinical examples providing evidence for dichotomous types of severity. , 1997, Archives of dermatology.

[58]  J. Ono,et al.  Regional cortical dysplasia associated with suspected hypomelanosis of Ito. , 1997, Pediatric neurology.

[59]  I. Febrer,et al.  LINEAR AND WHORLED NEVOID HYPERMELANOSIS , 1997, Pediatric dermatology.

[60]  A. Monaco,et al.  Characterisation of X; 17(q12;p 13) Translocation Breakpoints in a Female Patient with Hypomelanosis of Ito and Choroid Plexus Papilloma , 1997, European journal of human genetics : EJHG.

[61]  P. Frossard,et al.  Hypomelanosis of Ito may or may not involve hair growth. , 1997, Dermatology.

[62]  R. Happle.  Segmental forms of autosomal dominant skin disorders: different types of severity reflect different states of zygosity. , 1996, American journal of medical genetics.

[63]  J. S. Fryburg,et al.  Abnormal head MRI in a neurologically normal boy with hypomelanosis of Ito. , 1996, American journal of medical genetics.

[64]  K. Nehal,et al.  Analysis of 54 cases of hypopigmentation and hyperpigmentation along the lines of Blaschko. , 1996, Archives of dermatology.

[65]  J. Burford.  Linear and whorled naevoid hypermelanosis , 1996, The Australasian journal of dermatology.

[66]  E. Hatchwell.  Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis. , 1996, Journal of medical genetics.

[67]  E. Hatchwell,et al.  X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of Xp. , 1996, Journal of medical genetics.

[68]  I. Pascual‐Castroviejo,et al.  Arteriovenous malformation in hypomelanosis of Ito , 1996, Brain and Development.

[69]  M. Ruggieri,et al.  Involvement of the white matter in hypomelanosis of Ito (incontinentia pigmenti achromiens) , 1996, Neurology.

[70]  L. Braathen,et al.  Sporadic hypomelanosis of Ito with focal hypertrichosis in a 16-month-old girl. , 1996, Dermatology.

[71]  B. Echenne,et al.  Ito hypomelanosis and moyamoya disease. , 1995, Pediatric neurology.

[72]  A. Kanwar,et al.  Nevus Depigmentosus Associated with Hemihypertrophy of the Limhs , 1995, Pediatric dermatology.

[73]  G. Pini,et al.  Cerebellar involvement in hypomelanosis of Ito. , 1995, Neuropediatrics.

[74]  J. Savin,et al.  Dermatology and the New Genetics , 1995 .

[75]  A. Zvulunov,et al.  Neurocutaneous syndromes associated with pigmentary skin lesions. , 1995, Journal of the American Academy of Dermatology.

[76]  T. Hamada,et al.  Coexistence of generalized milia and naevus depigmentosus , 1995, The British journal of dermatology.

[77]  Y. Futagi,et al.  [Hypomelanosis of Ito associated with hemimegalencephaly]. , 1994, No to hattatsu = Brain and development.

[78]  V. Sybert.  Hypomelanosis of Ito: a description, not a diagnosis. , 1994, The Journal of investigative dermatology.

[79]  T. Ogino,et al.  Neurophysiologic dysfunction in hypomelanosis of Ito: EEG and evoked potential studies , 1994, Brain and Development.

[80]  J. García-Peñas,et al.  Incontinentia pigmenti: MR demonstration of brain changes. , 1994, AJNR. American journal of neuroradiology.

[81]  S. J. Orlow,et al.  Lines of Blaschko. , 1994, Journal of the American Academy of Dermatology.

[82]  R. Happle.  Mosaicism in human skin. Understanding the patterns and mechanisms. , 1993, Archives of dermatology.

[83]  M. Zappella,et al.  Autism and Hypomelanosis of Ito in Twins , 1993, Developmental medicine and child neurology.

[84]  K. Wakamatsu,et al.  Nevus Depigmentosus Systematicus With Partial Yellow Scalp Hair Due to Selective Suppression of Eumelanogenesis , 1993, Pediatric dermatology.

[85]  S. Larkins,et al.  Epidermal mosaicism and Blaschko's lines. , 1993, Journal of medical genetics.

[86]  S. Kihara,et al.  Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): further evidence of localization at Xp11. , 1993, American journal of medical genetics.

[87]  H. Ohashi,et al.  Pigmentary dysplasias and chromosomal mosaicism: report of 9 cases. , 1992, American journal of medical genetics.

[88]  C. Ensinger,et al.  Cytogenetic and dermatoglyphic findings in a familial case of hypomelanosis of Ito (incontinentia pigmenti achromians) , 1992, Clinical genetics.

[89]  A. Read,et al.  Hypomelanosis of Ito , 1992, The Lancet.

[90]  S. Toussaint,et al.  Hypomelanosis of Ito: Diagnostic Criteria and Report of 41 Cases , 1992, Pediatric dermatology.

[91]  Esquivel Ee,et al.  EEG findings in hypomelanosis of Ito. , 1991 .

[92]  A. Calabrò,et al.  Hypomelanosis of Ito associated with chromosomal translocation involving Xp11. , 1991, American journal of medical genetics.

[93]  C. Gillberg,et al.  Hypomelanosis of Ito in Three Cases with Autism and Autistic‐like Conditions , 1991, Developmental medicine and child neurology.

[94]  A. Baruzzi,et al.  Familial hypomelanosis of Ito. , 1991, European neurology.

[95]  A. Elster,et al.  Cranial MR imaging in hypomelanosis of Ito. , 1990, Journal of computer assisted tomography.

[96]  R. Pagon,et al.  Pigmentary abnormalities and mosaicism for chromosomal aberration: association with clinical features similar to hypomelanosis of Ito. , 1990, The Journal of pediatrics.

[97]  D. Flannery.  Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism. , 1990, American journal of medical genetics.

[98]  W. Huk,et al.  Hypomelanosis of Ito (Incontinentia Pigmenti Achromians) , 1990 .

[99]  R. Kirnbauer,et al.  Ocular Symptomatology in Familial Hypomelanosis Ito , 1990 .

[100]  B. Cohen,et al.  Chromosome mosaicism in hypomelanosis of Ito. , 1990, American journal of medical genetics.

[101]  R. Happle.  [Absence of bipolarity in Blaschko's lines]. , 1990, Annales de dermatologie et de venereologie.

[102]  M. Hara,et al.  Ito Syndrome (Hypomelanosis of Ito) as a Cause of Intractable Epilepsy , 1989, The Japanese journal of psychiatry and neurology.

[103]  E. S. Cantú,et al.  Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism. , 1989, American journal of human genetics.

[104]  E. Brett,et al.  Hypomelanosis of Ito: spectrum of the disease. , 1989, The Journal of pediatrics.

[105]  V. Ramesh,et al.  HYPOMELANOSIS OF ITO: HISTOCHEMICAL AND ULTRASTRUCTURAL OBSERVATIONS , 1989, The Australasian journal of dermatology.

[106]  W. Griffiths,et al.  Linear and whorled nevoid hypermelanosis. , 1988, Journal of the American Academy of Dermatology.

[107]  A. Read,et al.  Hypomelanosis of Ito: a manifestation of mosaicism or chimerism. , 1988, Journal of medical genetics.

[108]  J. Burn,et al.  Genetic counselling in hypomelanosis of Ito: case report and review , 1988, Clinical genetics.

[109]  C. Herrero,et al.  Hypomelanosis of Ito. Neurological Complications in 34 Cases , 1988, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[110]  P. Battistella,et al.  Unilateral Hypomelanosis of Ito with Hemimegalencephaly , 1988, Acta paediatrica Scandinavica.

[111]  J. V. van Krieken,et al.  Malignant transformation in a naevus of Ito. A case report. , 1988, Histopathology.

[112]  E. Jabs,et al.  Single maxillary central incisor and coloboma in hypomelanosis of Ko , 1987, Clinical genetics.

[113]  W. Bell,et al.  Hypomelanosis of Ito. Wood's light and magnetic resonance imaging as diagnostic measures. , 1986, Archives of neurology.

[114]  A. Read,et al.  DIPLOID/TRIPLOID MIXOPLOIDY AND HYPOMELANOSIS OF ITO , 1986, The Lancet.

[115]  A. Kaplan,et al.  Hypomelanosis of Ito: neurologic complications. , 1986, Pediatric neurology.

[116]  T. Katoh,et al.  Hypomelanosis of Itō associated with benign tumors and chromosomal abnormalities: A neurocutaneous syndrome , 1985, Brain and Development.

[117]  R. Happle,et al.  [How are the Blaschko lines arranged on the scalp?]. , 1984, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

[118]  S. Rosemberg,et al.  Hypomelanosis of Ito. Case report with involvement of the central nervous system and review of the literature. , 1984, Neuropediatrics.

[119]  A. Metzker,et al.  Segmental pigmentation disorder. , 1983, Acta dermato-venereologica.

[120]  B. Liwnicz,et al.  Hypomelanosis of Ito (incontinentia pigmenti achromians)—a clinicopathologic study , 1982, Neurology.

[121]  E. Feuerman,et al.  [Incontinentia pigmenti achromians (systematized depigmented nevus)]. , 1982, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

[122]  R. Happle,et al.  Hamartomatous dental cusps in hypomelanosis of Ito , 1982, Clinical genetics.

[123]  T. David.  Hypomelanosis of Itô: a neurocutaneous syndrome. , 1981, Archives of disease in childhood.

[124]  S. Ohdo,et al.  Incontinentia pigmenti achromians as part of a neurocutaneous syndrome: A case report , 1979, Brain and Development.

[125]  Y. Setoguchi,et al.  A malformation complex of ectrodactyly, clefting and hypomelanosis of ito (incontinentia pigmenti achromians). , 1979, The Cleft palate journal.

[126]  J. Ortonne,et al.  [Hypomelanosis of Ito: report of one case (author's transl)]. , 1979, Annales de dermatologie et de venereologie.

[127]  R. Tan.  (11) Incontinentia pigmenti achromians (hypomelanosis of Ito) , 1977 .

[128]  A. Dupré,et al.  [Incontinentia pigmenti achromians of Ito]. , 1977, Annales de dermatologie et de venereologie.

[129]  M. Morohashi,et al.  Ultrastructural studies of vitiligo, Vogt-Koyanagi syndrome, and incontinentia pigmenti achromians. , 1977, Archives of dermatology.

[130]  A. González-mendoza,et al.  INCONTINENTIA PIGMENTI ACHROMIANS (ITO'S HYPOMELANOSIS) , 1977, International journal of dermatology.

[131]  D. Fretzin,et al.  Hypomelanosis of Ito (incontinentia pigmenti achromians): a neurocutaneous syndrome. , 1977, The Journal of pediatrics.

[132]  R. Jackson.  The lines of Blaschko: a review and reconsideration , 1976, The British journal of dermatology.

[133]  R. Browne,et al.  Dental dysplasia in incontinentia pigmenti achromians (Ito). An unusual form , 1976, British Dental Journal.

[134]  A. Griffiths,et al.  Incontinentia pigmenti achromians. , 1975, Archives of dermatology.

[135]  T. Fitzpatrick,et al.  Congenital circumscribed hypomelanosis: a characterization based on electron microscopic study of tuberous sclerosis, nevus depigmentosus, and piebaldism. , 1975, The Journal of investigative dermatology.

[136]  Conant Ma,et al.  Proceedings: Unilateral systematized hypochromic nevus. , 1974 .

[137]  R. Bart,et al.  Hypomelanosis of Ito ("incontinentia pigmenti achromians"). Report of three cases and review of the literature. , 1973, Archives of dermatology.

[138]  J. Maize,et al.  Systematized hypochromic nevus. Incontinentia pigmenti achromians of Ito. , 1972, Archives of dermatology.

[139]  M. Rubin.  Incontinentia pigmenti achromians. Multiple cases within a family. , 1972, Archives of Dermatology.

[140]  P. Stoebner,et al.  Incontinentia pigmenti achromians (ITO). Etude clinique et histo-pathologique. , 1971 .

[141]  E. Grosshans,et al.  Incontinentia pigmenti achromians(ITO) , 1971 .

[142]  P. Stoebner,et al.  [Incontinentia pigmenti achromians (ITO). An ultrastructural study]. , 1970, Archiv fur klinische und experimentelle Dermatologie.

[143]  T. Hamada,et al.  "Incontinentia pigmenti achromians (Ito)". , 1967, Archives of dermatology.