162 related articles for article (PubMed ID: 25201868)
1. CHILD syndrome.
Heda GD; Valivade V; Sanghavi P; Kukreja RM; Phulari YJ
Indian J Dermatol Venereol Leprol; 2014; 80(5):483. PubMed ID: 25201868
[No Abstract] [Full Text] [Related]
2. Optic nerve findings in CHILD syndrome.
Knape RM; Gandhi KB; Tuli SY; Khuddus N
J Pediatr Ophthalmol Strabismus; 2010 Sep; 47 Online():e1-3. PubMed ID: 20886807
[TBL] [Abstract][Full Text] [Related]
3. Unilateral Erythematous Lesions with Wax-like Scaling and Limb Abnormalities: A Quiz.
Lelonek E; Matusiak Ł; Bieniek A; Szepietowski JC
Acta Derm Venereol; 2016 Nov; 96(7):1004-1008. PubMed ID: 26832123
[No Abstract] [Full Text] [Related]
4. A novel X-chromosomal microdeletion encompassing congenital hemidysplasia with ichthyosiform erythroderma and limb defects.
Raychaudhury T; George R; Mandal K; Srivastava VM; Thomas M; Bornholdt D; Grzeschik KH; Koehler A
Pediatr Dermatol; 2013; 30(2):250-2. PubMed ID: 22471832
[TBL] [Abstract][Full Text] [Related]
5. Mild clinical presentation of a patient with a mutation in the NSDHL gene.
Ormerod E; Bownass L; Smithson S; Zhang Y; Dunnill MGS
Clin Exp Dermatol; 2019 Jun; 44(4):456-458. PubMed ID: 30488480
[No Abstract] [Full Text] [Related]
6. Verrucous hyperkeratosis with predominant involvement of the left side of the body and concomitant onychodystrophy in a 17-year-old girl.
Armina S; Heiko T; Rudolf H; Judith F; Dimitra K; Peter S
J Dtsch Dermatol Ges; 2020 Sep; 18(9):1054-1057. PubMed ID: 32515052
[No Abstract] [Full Text] [Related]
7. CHILD syndrome: effective treatment of ichthyosiform naevus with oral and topical ketoconazole.
Liu T; Qian G; Wang XX; Zhang YG
Acta Derm Venereol; 2015 Jan; 95(1):91-2. PubMed ID: 24696032
[No Abstract] [Full Text] [Related]
8. CHILD syndrome with mild skin lesions: histopathologic clues for the diagnosis.
Gantner S; Rütten A; Requena L; Gassenmaier G; Landthaler M; Hafner C
J Cutan Pathol; 2014 Oct; 41(10):787-90. PubMed ID: 25093865
[TBL] [Abstract][Full Text] [Related]
9. CHILD syndrome mimicking verrucous nevus in a Chinese patient responded well to the topical therapy of compound of simvastatin and cholesterol.
Yu X; Zhang J; Gu Y; Deng D; Wu Z; Bao L; Li M; Yao Z
J Eur Acad Dermatol Venereol; 2018 Jul; 32(7):1209-1213. PubMed ID: 29341259
[TBL] [Abstract][Full Text] [Related]
10. Hyperkeratotic Nodule on the Knee in a Patient With KID Syndrome.
Chou P; Lee M; Elsensohn A
Cutis; 2024 Mar; 113(3):118-124. PubMed ID: 38648589
[No Abstract] [Full Text] [Related]
11. CHILD syndrome: A modified pathogenesis-targeted therapeutic approach.
Bergqvist C; Abdallah B; Hasbani DJ; Abbas O; Kibbi AG; Hamie L; Kurban M; Rubeiz N
Am J Med Genet A; 2018 Mar; 176(3):733-738. PubMed ID: 29392821
[TBL] [Abstract][Full Text] [Related]
12. Novel
Maceda EBG; Kratz LE; Ramos VME; Abacan MAR
BMJ Case Rep; 2020 Nov; 13(11):. PubMed ID: 33139364
[TBL] [Abstract][Full Text] [Related]
13. Multiple verruciform xanthomas in the setting of congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome.
Xu XL; Huang LM; Wang Q; Sun JF
Pediatr Dermatol; 2015; 32(1):135-7. PubMed ID: 24147604
[TBL] [Abstract][Full Text] [Related]
14. CHILD Syndrome: Case Report of a Chinese Patient and Literature Review of the NAD[P]H Steroid Dehydrogenase-Like Protein Gene Mutation.
Mi XB; Luo MX; Guo LL; Zhang TD; Qiu XW
Pediatr Dermatol; 2015; 32(6):e277-82. PubMed ID: 26459993
[TBL] [Abstract][Full Text] [Related]
15. Congenital hemidysplasia with ichthyosiform naevus and limb defects (CHILD) syndrome without hemidysplasia.
Estapé A; Josifova D; Rampling D; Glover M; Kinsler VA
Br J Dermatol; 2015 Jul; 173(1):304-7. PubMed ID: 25533639
[No Abstract] [Full Text] [Related]
16. CHILD syndrome with minimal limb abnormalities.
Noguera-Morel L; Hernández-Ostiz S; Casas-Fernández L; Hernández-Martín A; Rodríguez-Blanco I; Requena L; Hotz A; Fischer J; Torrelo A
J Eur Acad Dermatol Venereol; 2016 Dec; 30(12):e201-e202. PubMed ID: 26611379
[No Abstract] [Full Text] [Related]
17. CHILD syndrome with thrombocytosis and congenital dislocation of hip: A case report from India.
Chander R; Varghese B; Jabeen M; Garg T; Jain M
Dermatol Online J; 2010 Aug; 16(8):6. PubMed ID: 20804683
[TBL] [Abstract][Full Text] [Related]
18. CHILD syndrome caused by a deletion of exons 6-8 of the NSDHL gene.
Kim CA; Konig A; Bertola DR; Albano LM; Gattás GJ; Bornholdt D; Leveleki L; Happle R; Grzeschik KH
Dermatology; 2005; 211(2):155-8. PubMed ID: 16088165
[TBL] [Abstract][Full Text] [Related]
19. Large deletions in the NSDHL gene in two patients with CHILD syndrome.
Yang Z; Hartmann B; Xu Z; Ma L; Happle R; Schlipf N; Zhang LX; Xu ZG; Wang ZY; Fischer J
Acta Derm Venereol; 2015 Nov; 95(8):1007-8. PubMed ID: 26014843
[No Abstract] [Full Text] [Related]
20. A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next-generation sequencing causes CK syndrome.
Preiksaitiene E; Caro A; Benušienė E; Oltra S; Orellana C; Morkūnienė A; Roselló MP; Kasnauskiene J; Monfort S; Kučinskas V; Mayo S; Martinez F
Am J Med Genet A; 2015 Jun; 167(6):1342-8. PubMed ID: 25900314
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]