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Quoted phrase not found in phrase index: "Severe achondroplasia-developmental delay-acanthosis nigricans syndrome"
Page 1
Acanthosis nigricans and the metabolic syndrome.
Karadağ AS, You Y, Danarti R, Al-Khuzaei S, Chen W. Karadağ AS, et al. Clin Dermatol. 2018 Jan-Feb;36(1):48-53. doi: 10.1016/j.clindermatol.2017.09.008. Epub 2017 Sep 8. Clin Dermatol. 2018. PMID: 29241752 Review. No abstract available.
Obesity and dermatology.
Scheinfeld NS. Scheinfeld NS. Clin Dermatol. 2004 Jul-Aug;22(4):303-9. doi: 10.1016/j.clindermatol.2004.01.001. Clin Dermatol. 2004. PMID: 15475230 Review.
It affects cutaneous sensation, temperature regulation, foot shape, and vasculature. Acanthosis nigricans is the most common dermatological manifestation of obesity. ...Leg ulcerations, lymphedema, plantar hyperkeratosis, and striae are more common with obesity. Hormonal a …
It affects cutaneous sensation, temperature regulation, foot shape, and vasculature. Acanthosis nigricans is the most common dermatol …
A-type lamin-linked lipodystrophies.
Vigouroux C, Capeau J. Vigouroux C, et al. Novartis Found Symp. 2005;264:166-77; discussion 177-82, 227-30. Novartis Found Symp. 2005. PMID: 15773753 Review.
Genetic forms of partial lipodystrophy are currently recognized as two syndromes with subcutaneous lipoatrophy but preserved or increased fat at the level of face and neck (Dunnigan syndrome or FPLD due to LMNA mutations) and/or abdomen (PPARgamma-linked forms) and …
Genetic forms of partial lipodystrophy are currently recognized as two syndromes with subcutaneous lipoatrophy but preserved or incre …
The clinical evaluation of hirsutism.
Somani N, Harrison S, Bergfeld WF. Somani N, et al. Dermatol Ther. 2008 Sep-Oct;21(5):376-91. doi: 10.1111/j.1529-8019.2008.00219.x. Dermatol Ther. 2008. PMID: 18844715 Review.
Other cutaneous conditions associated with androgen excess are androgenetic alopecia, acanthosis nigricans, and acne. Hirsutism is often associated with measurably elevated androgen levels, but not in all cases. ...Other causes are late onset congenital adrenal hyperplasia …
Other cutaneous conditions associated with androgen excess are androgenetic alopecia, acanthosis nigricans, and acne. Hirsutism is of …
Hyperinsulinemia and ovarian hyperandrogenism. Cause and effect.
Barbieri RL, Hornstein MD. Barbieri RL, et al. Endocrinol Metab Clin North Am. 1988 Dec;17(4):685-703. Endocrinol Metab Clin North Am. 1988. PMID: 3058472 Review.
The most dramatic clinical expression of the association between hyperinsulinemia and hyperandrogenism is the HAIR-AN syndrome. In the HAIR-AN syndrome, severe insulin resistance results in a compensatory hyperinsulinemia that stimulates ovarian androgen prod …
The most dramatic clinical expression of the association between hyperinsulinemia and hyperandrogenism is the HAIR-AN syndrome. In th …
Cardiometabolic risk factors among children who are affected by overweight, obesity and severe obesity.
Nur Zati Iwani AK, Jalaludin MY, Roslan FA, Mansor F, Md Zain F, Hong JYH, Zin RMWM, Yahya A, Ishak Z, Selamat R, Mokhtar AH. Nur Zati Iwani AK, et al. Front Public Health. 2023 Apr 27;11:1097675. doi: 10.3389/fpubh.2023.1097675. eCollection 2023. Front Public Health. 2023. PMID: 37181686 Free PMC article.
BACKGROUND: The increasing severity of obesity is expected to lead to more serious health effects. ...RESULTS: Out of 924 children, 38.4% (n = 355) were overweight, 43.6% (n = 403) were obese, and 18% (n = 166) were severely obese. The overall mean age was 9.9 0.8 y …
BACKGROUND: The increasing severity of obesity is expected to lead to more serious health effects. ...RESULTS: Out of 924 children, 3 …
Rabson-Mendenhall Syndrome in a brother-sister pair in Kuwait: Diagnosis and 5 year follow up.
Al-Kandari H, Al-Abdulrazzaq D, Al-Jaser F, Al-Mulla F, Davidsson L. Al-Kandari H, et al. Prim Care Diabetes. 2021 Feb;15(1):175-177. doi: 10.1016/j.pcd.2020.07.012. Epub 2020 Aug 23. Prim Care Diabetes. 2021. PMID: 32843252
AIM: To report on Rabson-Mendenhall Syndrome (RMS) diagnosed in Kuwait. METHODS: A toddler (18 months old) was referred with high plasma insulin and dysmorphic features suggestive of RMS including coarse facial features with globular nose, full lips and furrowed tongue. .. …
AIM: To report on Rabson-Mendenhall Syndrome (RMS) diagnosed in Kuwait. METHODS: A toddler (18 months old) was referred with high pla …
Acanthosis nigricans: a new cutaneous sign in severe atopic dermatitis and Down syndrome.
Muñoz-Pérez MA, Camacho F. Muñoz-Pérez MA, et al. J Eur Acad Dermatol Venereol. 2001 Jul;15(4):325-7. J Eur Acad Dermatol Venereol. 2001. PMID: 11730043
To our knowledge, the association of AN with severe atopic dermatitis (AD) or Down syndrome has not been described before. This 82-month retrospective study included 1038 patients: AN was present in 4.9% of atopic patients and 50.9% of subjects with Down syndrome …
To our knowledge, the association of AN with severe atopic dermatitis (AD) or Down syndrome has not been described before. Thi …
Clinical signs, interventions, and treatment course of three different treatment protocols in patients with Crouzon syndrome with acanthosis nigricans.
de Planque CA, Wall SA, Dalton L, Paternoster G, Arnaud É, van Veelen MC, Versnel SL, Johnson D, Jayamohan J, Mathijssen IMJ. de Planque CA, et al. J Neurosurg Pediatr. 2021 Aug 13;28(4):425-431. doi: 10.3171/2021.2.PEDS20933. J Neurosurg Pediatr. 2021. PMID: 34388723
OBJECTIVE: Crouzon syndrome with acanthosis nigricans (CAN) is a rare and clinically complex subtype of Crouzon syndrome. ...CONCLUSIONS: This study demonstrates that patients with the mutation c.1172C>A (p.Ala391Glu) in the FGFR3 gene have a severe …
OBJECTIVE: Crouzon syndrome with acanthosis nigricans (CAN) is a rare and clinically complex subtype of Crouzon syndrome …
Molecular diagnosis of bilateral coronal synostosis.
Mulliken JB, Steinberger D, Kunze S, Müller U. Mulliken JB, et al. Plast Reconstr Surg. 1999 Nov;104(6):1603-15. doi: 10.1097/00006534-199911000-00001. Plast Reconstr Surg. 1999. PMID: 10541159 Review.
Twenty-five patients were diagnosed as having either Crouzon or Pfeiffer syndrome. Five patients with Crouzon syndrome of variable severity had mutations in exon 7 of FGFR2. ...A wide phenotypic range was observed in patients with identical mutations, includi …
Twenty-five patients were diagnosed as having either Crouzon or Pfeiffer syndrome. Five patients with Crouzon syndrome of vari …
62 results