María del C Boente

Summary

Country: Argentina

Publications

  1. doi Cutis tricolor parvimaculata in two patients with ring chromosome 15 syndrome
    Maria del Carmen Boente
    Department of Dermatology, Hospital del Nino Jesus, Tucuman, Argentina
    Pediatr Dermatol 28:670-3. 2011
  2. ncbi Pronounced linear calcinosis in a boy with mild dermatomyositis. A further possible example of superimposed segmental manifestation of a polygenic disorder
    Maria del Carmen Boente
    Department of Dermatology, Hospital del Nino Jesus, Tucuman, Argentina
    Dermatology 219:155-7. 2009
  3. ncbi [Dermatopathy associated with levamisole-induced reversible posterior leukoencephalopathy]
    María del C Boente
    Servicio de Dermatologia, Hospital del Nino Jesus, Tucuman, Argentina
    Arch Argent Pediatr 106:42-6. 2008
  4. doi Cutis tricolor coexistent with cutis marmorata telangiectatica congenita: "phacomatosis achromico-melano-marmorata"
    María del C Boente
    Department of Dermatology, Hospital del Nino Jesus, Pasaje Bertres 224, SM de Tucumán, Argentina
    Eur J Dermatol 18:394-6. 2008
  5. ncbi Phacomatosis pigmentokeratotica: a follow-up report documenting additional cutaneous and extracutaneous anomalies
    Maria del Carmen Boente
    Department of Dermatology, Hospital del Nino Jesus, Tucuman, Argentina
    Pediatr Dermatol 25:76-80. 2008
  6. ncbi Focal dermal hypoplasia: ultrastructural abnormalities of the connective tissue
    María del Carmen Boente
    Servicio de Dermatologia, Hospital del Nino Jesus, Tucuman, Argentina
    J Cutan Pathol 34:181-7. 2007
  7. ncbi Geroderma osteodysplastica. Report of a new family
    Maria del Carmen Boente
    Servicio de Dermatologia, Hospital del Nino Jesus, Tucuman, Argentina
    Pediatr Dermatol 23:467-72. 2006
  8. ncbi Desmoplastic hairless hypopigmented nevus (DHHN). A distinct variant of giant melanocytic nevus
    Maria del Carmen Boente
    Centro de Investigaciones Dermatológicas, Tucuman, Argentina
    Eur J Dermatol 15:451-3. 2005
  9. ncbi [Linear Darier disease in two siblings. An example of loss of heterozygosity]
    M del C Boente
    Departement de Dermatologie, Hôpital del Nino Jesus, Pasaje Bertre 224 SM de Tucuman 4000, Tucuman, Argentina
    Ann Dermatol Venereol 131:805-9. 2004
  10. ncbi Familial cutaneous collagenoma: a clinicopathologic study of two new cases
    María del C Boente
    Department of Dermatology, Hospital del Nino Jesus, Argentina
    Pediatr Dermatol 21:33-8. 2004

Collaborators

Detail Information

Publications13

  1. doi Cutis tricolor parvimaculata in two patients with ring chromosome 15 syndrome
    Maria del Carmen Boente
    Department of Dermatology, Hospital del Nino Jesus, Tucuman, Argentina
    Pediatr Dermatol 28:670-3. 2011
    ..Future clinical research may show whether analogous "simple" twin-spot phenotypes in the form of cutis tricolor parvimaculata may be considered a further cutaneous sign of the ring chromosome 15 syndrome...
  2. ncbi Pronounced linear calcinosis in a boy with mild dermatomyositis. A further possible example of superimposed segmental manifestation of a polygenic disorder
    Maria del Carmen Boente
    Department of Dermatology, Hospital del Nino Jesus, Tucuman, Argentina
    Dermatology 219:155-7. 2009
    ..Either LOH or a postzygotic mutation at an additional gene locus may explain the pronounced linear involvement...
  3. ncbi [Dermatopathy associated with levamisole-induced reversible posterior leukoencephalopathy]
    María del C Boente
    Servicio de Dermatologia, Hospital del Nino Jesus, Tucuman, Argentina
    Arch Argent Pediatr 106:42-6. 2008
    ..We present a 9-years old girl who developed a cutaneous eruption and a reverse leucoencephalopathy with a short treatment but high doses of the drug...
  4. doi Cutis tricolor coexistent with cutis marmorata telangiectatica congenita: "phacomatosis achromico-melano-marmorata"
    María del C Boente
    Department of Dermatology, Hospital del Nino Jesus, Pasaje Bertres 224, SM de Tucumán, Argentina
    Eur J Dermatol 18:394-6. 2008
    ..Future clinical research may show whether analogous "simple" twin-spot phenotypes in the form of "phacomatosis melanomarmorata" or "phacomatosis achromicomarmorata" do likewise exist...
  5. ncbi Phacomatosis pigmentokeratotica: a follow-up report documenting additional cutaneous and extracutaneous anomalies
    Maria del Carmen Boente
    Department of Dermatology, Hospital del Nino Jesus, Tucuman, Argentina
    Pediatr Dermatol 25:76-80. 2008
    ....
  6. ncbi Focal dermal hypoplasia: ultrastructural abnormalities of the connective tissue
    María del Carmen Boente
    Servicio de Dermatologia, Hospital del Nino Jesus, Tucuman, Argentina
    J Cutan Pathol 34:181-7. 2007
    ..Taking into account that a common link between all laminopaties may be a failure of stem cells to regenerate mesenchymal tissue, this failure would induce the dermal hypoplasia observed in our patients presenting Goltz syndrome...
  7. ncbi Geroderma osteodysplastica. Report of a new family
    Maria del Carmen Boente
    Servicio de Dermatologia, Hospital del Nino Jesus, Tucuman, Argentina
    Pediatr Dermatol 23:467-72. 2006
    ..We consider the differential diagnosis with other syndromes associated with cutis laxa using clinical, radiologic, and histopathologic criteria...
  8. ncbi Desmoplastic hairless hypopigmented nevus (DHHN). A distinct variant of giant melanocytic nevus
    Maria del Carmen Boente
    Centro de Investigaciones Dermatológicas, Tucuman, Argentina
    Eur J Dermatol 15:451-3. 2005
    ..Immunostaining revealed S100 +, Vim +, HMB45--results. The nevus has continued to involute to date. An immune response against the melanocytes of the nevus may explain this type of evolution...
  9. ncbi [Linear Darier disease in two siblings. An example of loss of heterozygosity]
    M del C Boente
    Departement de Dermatologie, Hôpital del Nino Jesus, Pasaje Bertre 224 SM de Tucuman 4000, Tucuman, Argentina
    Ann Dermatol Venereol 131:805-9. 2004
    ..We present two siblings affected with the linear form of this disorder and discuss these cases as an example of the genetic mechanism of loss of heterozygosity...
  10. ncbi Familial cutaneous collagenoma: a clinicopathologic study of two new cases
    María del C Boente
    Department of Dermatology, Hospital del Nino Jesus, Argentina
    Pediatr Dermatol 21:33-8. 2004
    ..The diagnosis was therefore confirmed to be connective tissue nevi of the collagen type. The differential diagnosis of connective tissue nevi disorders is delineated...
  11. ncbi Linear porokeratosis associated with disseminated superficial actinic porokeratosis: a new example of type II segmental involvement
    Maria del Carmen Boente
    Centro de Investigaciones Dermatológicas, Tucuman, Argentina
    Pediatr Dermatol 20:514-8. 2003
    ..This case is also important for molecular studies because of the presence of heterozygous and homozygous mutated cells in the same patient and the familial occurrence of the heterozygous form of the disease...
  12. ncbi Costello syndrome: report of a new case with choanal atresia and fatal outcome
    M C Boente
    Dermatology Division Hospital del Niño Jésùs, Facultad de Medicina, UNT, Tucuman, Argentina
    Eur J Dermatol 11:453-7. 2001
    ..The differential diagnosis of cutis laxa in association with postnatal growth retardation and developmental delay and with cardio-facio-cutaneous and Noonan syndromes is discussed...
  13. ncbi Nevus psiloliparus and aplasia cutis: a further possible example of didymosis
    Antonio Torrelo
    Department of Dermatology, Hospital del Nino Jesus, Madrid, Spain
    Pediatr Dermatol 22:206-9. 2005
    ..This unusual association may be considered a further example of didymosis, for which we propose the term, didymosis aplasticopsilolipara...