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710 Possible Causes for Congenital Alopecia, Pediatric Disorder

  • Congenital Syphilis

    In this article, we describe the first occurrence of alopecia in a neonate with congenital syphilis.[ncbi.nlm.nih.gov] Rhinitis with highly infectious nasal discharge, nontender generalized adenopathy, alopecia, iritis, and failure to thrive occur less frequently.[dartmouth.edu] Neonatal alopecia has been described in many circumstances but never as a part of the constellation of signs in congenital syphilis.[ncbi.nlm.nih.gov]

  • Congenital Alopecia

    Frieden, two of the most important names in the fields of dermatology and pediatrics.[books.google.com] We present the first case of cutaneous mastocytosis associated with congenital alopecia areata in a 3-year-old Korean girl.[ncbi.nlm.nih.gov] Key words: alopecia; disorders; gentrichosis; hair growth; hypotrichosis World J Pediatr 2011;7(2):111-117 Introduction There have been numerous attempts to classify the conditions[wjpch.com]

  • Zinc Deficiency

    Malnutrition, prematurity, total parenteral nutrition dependence, and burns increase the demand for zinc, whereas congenital malabsorption syndromes represent clinical situations[ncbi.nlm.nih.gov] Anxiety in Children In our practice, in addition to zinc deficiency, we often see yeast issues and gut issues in our pediatric patients with general anxiety disorder.[mensahmedical.com] […] hyperactivity disorder EFA — essential fatty acids EPD — enzyme-potentiated desensitization IGg — immunoglobulin G LC — long chain PUFA — polyunsaturated fatty acids Accepted[doi.org]

  • Juvenile Polyp

    Wireless capsule endoscopy for oscure small-bowel disorders: Final results of the first pediatric controlled trial . Clin Gastroenterol Hepatol 2005; 3 :264–270. 21.[nature.com] ), bone (hypertelorism, bone cysts, congenital cleft lip and palate), brain Figure 4.[file.scirp.org] […] fifth finger clubbed fingers and retrognathia. in fact, patients with juvenile polyposis can have many extra-digestive abnormalities [3]: cutaneous (telangiectasia, nevus, alopecia[file.scirp.org]

  • Nevus Sebaceous

    Author information 1 Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.[ncbi.nlm.nih.gov] Differential Diagnosis (Other conditions with similar appearance) Aplasia cutis congenita Juvenile xanthogranulomas Mastocytomas Congenital triangular alopecia Diagnosis Key[ozarkderm.com] […] abnormality that can lead to cosmetic deformity, alopecia, or malignant transformation in rare circumstances.[ncbi.nlm.nih.gov]

  • Rasmussen Syndrome

    Recognition of the syndrome, especially in pediatric populations, is difficult and often undiagnosed and/or confused with neurological disorders with similar clinical features[ncbi.nlm.nih.gov] A 9-year-old boy diagnosed as having Rasmussen syndrome had congenital IgA deficiency and juvenile alopecia.[ncbi.nlm.nih.gov] […] work in the neurosciences, genetics, electroencephalography, pediatric and adult neurology, neuropharmacology, neurosurgery, and psychiatry.[books.google.com]

  • Congenital Ichthyosis

    A syndrome with severe generalized congenital ichthyosis, alopecia, eclabion, ectropion and mental retardation without neurological symptoms or macular changes in the eyes[ncbi.nlm.nih.gov] Turk J Pediatr 2017; 59: 475-482.[ncbi.nlm.nih.gov] Traupe H, Happle R (1983) Alopecia ichthyotica. A characteristic feature of congenital ichthyosis. Dermatologica 167:225–230 Google Scholar 11.[link.springer.com]

  • Juvenile Paralysis Agitans of Hunt

    […] see Chap. 37 ), birth injuries, epilepsy, disharmonies of development, and learning disabilities (see Chap. 27 )—make up the bulk of the clinical problems with which the pediatric[accessmedicine.mhmedical.com] alopecia, and nail dystrophy 006857 Frem2 Frem2 ne no eyelid eye, skeleton, coat color, kidney FREM2 Fraser syndrome 003613 Galc Galc twi-5J twitcher 5 Jackson neurological[jax.org] GENETIC ABERRATIONS AND INHERITANCE The diseases grouped in this chapter, and many in the next, represent four particular categories of genetic abnormality: (1) monogenic disorders[accessmedicine.mhmedical.com]

  • Brandt Syndrome

    Acrodermatitis enteropathica is a rare genetic disorder, especially in pediatric and dermatology clinics.[streetdirectory.com] Rupture of blisters expose the purulent eroded skin lesions. [1,2,4] Alopecia Diffuse hair loss in scalp, eye lashes and eye brows can be seen.[explainmedicine.com] A Comprehensive Guide to Acrodermatitis Enteropathica is the only book of its kind to give insight into this rare disorder.[blunck-medical-books.de]

  • Papillon Lefevre Disease

    alopecia and nail dystrophy TARP syndrome Trichohepatoenteric syndrome Tumor necrosis factor receptor-associated periodic syndrome Twin to twin transfusion syndrome Vici[rarediseases.info.nih.gov] Mucous membrane disorders. In: Pediatric Dermatology (Schachner LA, Hansen RC, eds), 1st Edn. New York: Churchill Livingstone, 1988; 482-3. 7. Carson EF.[ijdvl.com] Mancini, Hereditary Disorders of Cornification, Hurwitz Clinical Pediatric Dermatology, 10.1016/B978-1-4377-0412-9.00005-8, (92-114), (2011). R. Kumar and S.V.[doi.org]

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