CUSHING'S DISEASE AND POST-ADRENALECTOMY HYPERPIGMENTATION.
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17-Ketosteroids↗
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Results for “Pigmentation Disorders”
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
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Pigmented skin lesions in babies born to underweight former oral-contraceptive users.
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Contraceptives, Oral↗
[PROCEDURE TO FOLLOW IN THE CASE OF A BULLOUS DERMATOSIS IN A NEWBORN INFANT].
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Dermatitis, Exfoliative↗
POIKILODERMA CONGENITALE. (ROTHMUND--THOMSON SYNDROME).
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Bone Diseases↗
THE SYNDROMES OF TOTAL LIPODYSTROPHY AND OF PARTIAL LIPODYSTROPHY.
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Bone and Bones↗
[SKIN ATROPHY IN BANDS WITH GROWTH RETARDATION OF A LOWER EXTREMITY. RELATION TO SCLERODERMA AND LI'EVRE'S SPEDATROPHY].
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Adolescent↗
MELANOCYTE-STIMULATING HORMONE AND ADRENOCORTICOTROPHIC HORMONE. THEIR RELATION TO PIGMENTATION.
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Adrenalectomy↗
THE DISTRIBUTION OF CERTAIN GENES IN THE OLD ORDER AMISH.
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Amish↗
SYSTEMIC EFFECTS OF ANDROGENIC AND ESTROGENIC HORMONES IN ADVANCED BREAST CANCER.
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Androgens↗
THE INFLUENCE OF SALTS OF SOME HEAVY METALS ON OCCURRENCE OF PIGMENTARY CHANGES IN THE HAIRS OF ANIMALS FED BY POISONED MOTHERS.
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Animals, Newborn↗
ASYMMETRY, SHORT STATURE, AND VARIATIONS IN SEXUAL DEVELOPMENT. A SYNDROME OF CONGENITAL MALFORMATIONS.
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Birth Weight↗
HYPERPIGMENTATION ANDPITUITARY TUMOR AS SEQUELAE OF THE SURGICAL TREATMENT OF CUSHING'S SYNDROME.
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Adolescent↗
[ADDISON'S DISEASE: CHRONIC ADRENAL CORTEX INSUFFICIENCY].
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Addison Disease↗
THE AETIOLOGY OF KELOIDS: A REVIEW OF THE LITERATURE AND A NEW HYPOTHESIS.
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Acromegaly↗
UNIQUE SYNDROMES INVOLVING THE SKIN INDUCED BY DRUGS, FOOD ADDITIVES, AND ENVIRONMENTAL CONTAMINANTS.
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Aniline Compounds↗
PIGMENTATION IN ADDISON'S DISEASE; A CASE IN WHICH PIGMENTATION WAS THE ONLY SIGN.
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17-Ketosteroids↗
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.
Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal root and confluent eyebrows, heterochromia iridum, a white forelock and congenital deafness. The syndrome is inherited as a dominant, but affected individuals do not necessarily have all of the characteristics cited.Five hundred and fourteen pupils at a school for the deaf were screened for features of this syndrome. Three cases were discovered. Eleven other deaf children were found to have heterochromia iridum and two more had white forelocks. The interocular dimensions of the remaining children were recorded as standards by which to judge the presence of dystopia canthorum. The results of chromosomal analysis in two cases with Waardenburg's syndrome were normal.The findings provide further evidence that Waardenburg's syndrome is a distinct entity and call in question Mackenzie's concept of a comprehensive "first arch syndrome".
Adolescent↗