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Volumn 72, Issue 4, 2006, Pages 300-302
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Tuberous sclerosis complex associated with dyschromatosis universalis hereditaria
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Author keywords
Dyschromatosis universalis hereditaria; Tuberous sclerosis complex
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Indexed keywords
ADOLESCENT;
ARTICLE;
AUTOSOMAL DOMINANT DISORDER;
CASE REPORT;
CLINICAL FEATURE;
DEVELOPMENTAL DISORDER;
DIAGNOSTIC PROCEDURE;
DISEASE ASSOCIATION;
DYSCHONDROSTEOSIS;
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA;
ECHOCARDIOGRAPHY;
FAMILY HISTORY;
FEMALE;
FOOT SOLE;
GENE LOCUS;
GENE MUTATION;
GENERALIZED EPILEPSY;
GENODERMATOSIS;
HAMARTOMA;
HAND PALM;
HEMANGIOFIBROMA;
HISTOPATHOLOGY;
HUMAN;
HUMAN TISSUE;
HYPERPIGMENTATION;
HYPOPIGMENTATION;
IMAGE ANALYSIS;
MOUTH MUCOSA;
PHYSICAL EXAMINATION;
RHABDOMYOMA;
SKIN MACULE;
SYMPTOM;
TOOTH DISEASE;
TUBEROUS SCLEROSIS;
ADOLESCENT;
FEMALE;
FOOT DERMATOSES;
HAND DERMATOSES;
HUMANS;
MALE;
MOUTH MUCOSA;
PIGMENTATION DISORDERS;
SKIN DISEASES, GENETIC;
TUBEROUS SCLEROSIS;
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EID: 33746869673
PISSN: 03786323
EISSN: None
Source Type: Journal
DOI: 10.4103/0378-6323.26729 Document Type: Article |
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Times cited : (12)
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References (9)
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