Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anuja Sunkwad"'
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 2, Pp 84-87 (2020)
Brooke–Spiegler syndrome (BSS) is a rare autosomal dominant inherited disorder characterized by multiple skin appendageal tumors. The predominant tumors can be a cylindroma, trichoepithelioma, and/or spiradenoma. Here we report this rare entity of
Externí odkaz:
https://doaj.org/article/9c2811dfec29461c81a3c4e7ae3b46da
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 21, Iss 1, Pp 63-65 (2020)
Poikiloderma is characterized by mottled pigmentation, telangiectasia, and epidermal atrophy. It is a common cutaneous finding in a number of genodermatoses. We present a case of a 13-month-old male child with poikiloderma, heat intolerance, and phot
Externí odkaz:
https://doaj.org/article/5425de4982014736ada85655bb2df357
Autor:
Sunanda Mahajan, Anuja Sunkwad
Publikováno v:
International Journal of Contemporary Pediatrics. 8:1662
Background: Obesity currently is regarded as universal disease of epidemic prevalence and known as the evil of the twentieth century. The last 3 decades we have seen an unprecedented increase in the prevalence of obesity throughout the world includin
Autor:
Anuja Sunkwad, Vidya Kharkar
Publikováno v:
Indian Journal of Drugs in Dermatology, Vol 5, Iss 2, Pp 110-112 (2019)
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 21, Iss 1, Pp 63-65 (2020)
Poikiloderma is characterized by mottled pigmentation, telangiectasia, and epidermal atrophy. It is a common cutaneous finding in a number of genodermatoses. We present a case of a 13-month-old male child with poikiloderma, heat intolerance, and phot
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 7, Iss 2, Pp 84-87 (2020)
Brooke–Spiegler syndrome (BSS) is a rare autosomal dominant inherited disorder characterized by multiple skin appendageal tumors. The predominant tumors can be a cylindroma, trichoepithelioma, and/or spiradenoma. Here we report this rare entity of