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Quoted phrase not found in phrase index: "Congenital abnormal hair pattern"
Page 1
Hirsutism in Women.
Matheson E, Bain J. Matheson E, et al. Am Fam Physician. 2019 Aug 1;100(3):168-175. Am Fam Physician. 2019. PMID: 31361105 Free article. Review.
Hirsutism is the excessive growth of terminal hair in a typical male pattern in a female. It is often a sign of excessive androgen levels. ...Women with an abnormal hirsutism score based on the Ferriman-Gallwey scoring system should be ev …
Hirsutism is the excessive growth of terminal hair in a typical male pattern in a female. It is often a sign of excessive andr …
Hair loss in children.
Alves R, Grimalt R. Alves R, et al. Curr Probl Dermatol. 2015;47:55-66. doi: 10.1159/000369405. Epub 2015 Feb 20. Curr Probl Dermatol. 2015. PMID: 26370644 Review.
Hair loss is not uncommon in the pediatric group, but its patterns in this group are different from those seen in adults. ...Knowledge of the normal range and variation observed in the hair of children further enhances its assessment. This chapter has …
Hair loss is not uncommon in the pediatric group, but its patterns in this group are different from those seen in adults. ...K …
Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.
Moore SW. Moore SW. Pediatr Surg Int. 2012 Nov;28(11):1045-58. doi: 10.1007/s00383-012-3175-6. Epub 2012 Sep 23. Pediatr Surg Int. 2012. PMID: 23001136 Review.
It is characterized as a sex-linked heterogonous disorder with variable severity and incomplete penetrance giving rise to a variable pattern of inheritance. Although Hirschsprung's disease occurs as an isolated phenotype in at least 70% of cases, it is not infrequently ass …
It is characterized as a sex-linked heterogonous disorder with variable severity and incomplete penetrance giving rise to a variable patt …
Regional variability of modified Ferriman-Gallwey scorring in premenopausal healthy women in Southern Turkey.
Vural Solak GT, Akkus G, Solak Y, Kose S, Sert M. Vural Solak GT, et al. Gynecol Endocrinol. 2022 Aug;38(8):666-671. doi: 10.1080/09513590.2022.2096876. Epub 2022 Jul 8. Gynecol Endocrinol. 2022. PMID: 35801645
After these investigations, the women were divided into three groups according to the mF-G 8 score and evaluated. Group A (n = 59) had an mF-G 8 and, revealed an underlying disease causing hirsutism; group B (n = 42) had an mF-G 8, but no underlying disease responsible for …
After these investigations, the women were divided into three groups according to the mF-G 8 score and evaluated. Group A (n = 59) ha …
Molecular genetics of the hair follicle: the state of the art.
Van Steensel MA, Happle R, Steijlen PM. Van Steensel MA, et al. Proc Soc Exp Biol Med. 2000 Jan;223(1):1-7. doi: 10.1046/j.1525-1373.2000.22301.x. Proc Soc Exp Biol Med. 2000. PMID: 10632955 Review.
In a mere 5 years, the field has been revolutionized by the application of molecular genetics to human congenital skin disorders. Where dermatology first was limited to observation and empirics, there are now DNA-diagnostics, rational drug design, and perhaps even g …
In a mere 5 years, the field has been revolutionized by the application of molecular genetics to human congenital skin disorders. Whe …
Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literature.
Leclerc-Mercier S, Moshous D, Neven B, Mahlaoui N, Martin L, Pellier I, Blanche S, Picard C, Fischer A, Perot P, Eloit M, Fraitag S, Bodemer C. Leclerc-Mercier S, et al. J Eur Acad Dermatol Venereol. 2019 Jul;33(7):1412-1420. doi: 10.1111/jdv.15568. Epub 2019 Apr 15. J Eur Acad Dermatol Venereol. 2019. PMID: 30869812 Review.
The lesions presented as red-brownish nodules and infiltrated ulcerative plaques, predominantly on the face and limbs. Scleroderma-like infiltration on a single limb was observed in 10% of the cases. The associated PID was ataxia-telangiectasia (52%), combined immunodefici …
The lesions presented as red-brownish nodules and infiltrated ulcerative plaques, predominantly on the face and limbs. Scleroderma-like infi …
Behavioral profile in RASopathies.
Alfieri P, Piccini G, Caciolo C, Perrino F, Gambardella ML, Mallardi M, Cesarini L, Leoni C, Leone D, Fossati C, Selicorni A, Digilio MC, Tartaglia M, Mercuri E, Zampino G, Vicari S. Alfieri P, et al. Am J Med Genet A. 2014 Apr;164A(4):934-42. doi: 10.1002/ajmg.a.36374. Epub 2014 Jan 23. Am J Med Genet A. 2014. PMID: 24458522
Parents of 70 individuals with a RASopathy were asked to fill out the following questionnaires: Child Behavior Checklist (CBCL), Social Communication Questionnaire version lifetime (SCQ-L), and Modified Checklist for Autism in toddlers (M-CHAT). ...Our findings indicate th …
Parents of 70 individuals with a RASopathy were asked to fill out the following questionnaires: Child Behavior Checklist (CBCL), Soci …
Congenital cutaneous neurofibromas in neurofibromatosis type 1: Clinicopathological features in early infancy.
García-Martínez FJ, Azorín D, Duat-Rodríguez A, Hernández-Martín Á. García-Martínez FJ, et al. J Dtsch Dermatol Ges. 2021 Jan;19(1):73-80. doi: 10.1111/ddg.14322. Epub 2021 Jan 14. J Dtsch Dermatol Ges. 2021. PMID: 33448128
In twelve specimens we observed groups of fusiform cells arranged linearly mimicking a small caliber nerve trunk with abnormal morphology. Repeated biopsies from two of these lesions performed at different ages showed transformation to a plexiform pattern. An …
In twelve specimens we observed groups of fusiform cells arranged linearly mimicking a small caliber nerve trunk with abnormal …
Fibrodysplasia ossificans progressiva in Spain: epidemiological, clinical, and genetic aspects.
Morales-Piga A, Bachiller-Corral J, Trujillo-Tiebas MJ, Villaverde-Hueso A, Gamir-Gamir ML, Alonso-Ferreira V, Vázquez-Díaz M, Posada de la Paz M, Ayuso-García C. Morales-Piga A, et al. Bone. 2012 Oct;51(4):748-55. doi: 10.1016/j.bone.2012.07.002. Epub 2012 Jul 13. Bone. 2012. PMID: 22796417
In addition, other skeletal malformations such us fusion of the posterior elements of the cervical spine (89.0%), knee osteochondromas (71%), scoliosis (54.5%), and short and broad femoral neck (52.6%) were observed. All had developed mature ossicles of heterotopic bone in …
In addition, other skeletal malformations such us fusion of the posterior elements of the cervical spine (89.0%), knee osteochondromas (71%) …
Hair abnormality in Netherton syndrome observed under polarized light microscopy.
Utsumi D, Yasuda M, Amano H, Suga Y, Seishima M, Takahashi K. Utsumi D, et al. J Am Acad Dermatol. 2020 Sep;83(3):847-853. doi: 10.1016/j.jaad.2019.08.024. Epub 2020 Feb 3. J Am Acad Dermatol. 2020. PMID: 32029302
METHODS: Hairs obtained from 8 patients with Netherton syndrome were observed under polarized light, and we evaluated the correlation between number of band-like patterns and disease severity. RESULTS: Under polarized microscopy, the hair shafts of 8 patients …
METHODS: Hairs obtained from 8 patients with Netherton syndrome were observed under polarized light, and we evaluated the correlation …
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