Literature DB >> 22752729

Giant congenital melanocytic nevi: a rare association with hypophosphatemic rickets.

Geeta Gathwala, Poonam Dalal, Jagjit Singh Dalal, Surabhi Dayal, Gajendra Singh.   

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Year:  2012        PMID： 22752729     DOI： 10.1007/s12098-012-0802-0

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  5 in total

1.  Hypophosphatemic rickets with epidermal nevus syndrome.

Authors:  Mathew John; Nalini S Shah
Journal:  Indian Pediatr       Date:  2005-06       Impact factor: 1.411

Review 2.  Hypophosphatemic vitamin D-resistant rickets, precocious puberty, and the epidermal nevus syndrome.

Authors:  R Ivker; S D Resnick; R A Skidmore
Journal:  Arch Dermatol       Date:  1997-12

3.  Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets.

Authors:  A P Oranje; H Przyrembel; M Meradji; M C Loonen; J B de Klerk
Journal:  Arch Dermatol       Date:  1994-09

Review 4.  Physiological regulation and disorders of phosphate metabolism--pivotal role of fibroblast growth factor 23.

Authors:  Seiji Fukumoto
Journal:  Intern Med       Date:  2008-03-03       Impact factor: 1.271

5.  Linear sebaceous naevus syndrome and resistant rickets.

Authors:  H S Hosalkar; D H Jones; A Offiah; C Hall
Journal:  J Bone Joint Surg Br       Date:  2003-05
  5 in total
  3 in total

Review 1.  Cutaneous skeletal hypophosphatemia syndrome: clinical spectrum, natural history, and treatment.

Authors:  D Ovejero; Y H Lim; A M Boyce; R I Gafni; E McCarthy; T A Nguyen; L F Eichenfield; C M C DeKlotz; L C Guthrie; L L Tosi; P S Thornton; K A Choate; M T Collins
Journal:  Osteoporos Int       Date:  2016-08-06       Impact factor: 4.507

2.  Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia.

Authors:  Young H Lim; Diana Ovejero; Jeffrey S Sugarman; Cynthia M C Deklotz; Ann Maruri; Lawrence F Eichenfield; Patrick K Kelley; Harald Jüppner; Michael Gottschalk; Cynthia J Tifft; Rachel I Gafni; Alison M Boyce; Edward W Cowen; Nisan Bhattacharyya; Lori C Guthrie; William A Gahl; Gretchen Golas; Erin C Loring; John D Overton; Shrikant M Mane; Richard P Lifton; Moise L Levy; Michael T Collins; Keith A Choate
Journal:  Hum Mol Genet       Date:  2013-09-04       Impact factor: 6.150

Review 3.  DIAGNOSIS OF ENDOCRINE DISEASE: Mosaic disorders of FGF23 excess: Fibrous dysplasia/McCune-Albright syndrome and cutaneous skeletal hypophosphatemia syndrome.

Authors:  Luis F de Castro; Diana Ovejero; Alison M Boyce
Journal:  Eur J Endocrinol       Date:  2020-05       Impact factor: 6.664
  3 in total

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