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675 Possible Causes for Acanthosis Nigricans, Hirsutism, Kallmann Syndrome

  • Achard Thiers Syndrome

    Acanthosis nigricans is a common symptom of Achard Thiers syndrome as well.[symptoma.com] Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] Clinical features Achard–Thiers syndrome affects mostly postmenopausal women and comprises diabetes mellitus, deep voice, hirsutism or hypertrichosis, clitoral hypertrophy[ipfs.io]

  • Polycystic Ovary Syndrome

    Groups A and C showed increased frequency of acanthosis nigricans compared with Group B.[ncbi.nlm.nih.gov] 8 ( FGF8 ) Normosmic hypogonadotrophic hypogonadism and Kallmann syndrome (KAL6) 600483 [612702] Fibroblast growth factor receptor 1 ( FGFR1 ) Kallmann syndrome (KAL2) 136350[ncbi.nlm.nih.gov] Based on results of drug studies on hirsutism, a longer trial of several months may be required to clinically confirm the effects of spearmint tea on hirsutism. 10 In addition[ndnr.com]

  • HAIR-AN Syndrome

    , Acanthosis Nigricans} 進行詞彙精確檢索結果 出處/學術領域 英文詞彙 中文詞彙 學術名詞 醫學名詞 HAIR-AN syndrome{HyperAndrogenism, Insulin, Resistance, Acanthosis Nigricans} HAIR-AN症候群{雄性激素過多、胰島素抗性、黑色棘皮症}[terms.naer.edu.tw] […] make-up syndrome Kallmann's syndrome Kanzaki's disease Kasabach-Merritt syndrome Kawasaki's disease KID syndrome Kimura's disease Kindler syndrome Kitamura's reticulate acropigmentation[rr2.nakayamashoten.co.jp] The most common cause of hirsutism is polycystic ovarian syndrome. Patients with "idiopathic" hirsutism have normal ovulatory cycles and androgen levels.[ncbi.nlm.nih.gov]

  • Patterson Pseudoleprechaunism Syndrome

    The type A syndrome of insulin resistance and acanthosis nigricans showed no abnormality of EGF receptor ... Clinical Synopsis ...[ibis-birthdefects.org] Kahrizi syndrome Kaler Garrity Stern Syndrome Kallmann syndrome Kantaputra Gorlin Syndrome Kaplan Plauchu Fitch Syndrome Kaplowitz Bodurtha syndrome Kapur Toriello Syndrome[rgd.mcw.edu] […] adrenal disorder characterized by congenital bronzed hyperpigmentation, cutis laxa of the hands and feet, body disproportion (comprising large hands, feet, nose and ears), hirsutism[orpha.net]

  • Primary Amenorrhea

    nigricans, higher diastolic blood pressure, and lower high-density lipoprotein cholesterol level).[ncbi.nlm.nih.gov] All of these features suggested Kallmann syndrome. This syndrome commonly presents with delayed onset of puberty and decreased or absent sense of smell.[ncbi.nlm.nih.gov] Hirsutism and clitoromegaly were present. Ultrasound examination showed polycystic appearance of the ovary.[ncbi.nlm.nih.gov]

  • Acquired Adrenogenital Syndrome

    Many women with the disorder have acanthosis nigricans.[rarediseases.org] Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.de] True hirsutism is distinct from hypertrichosis, which is simply an excessive feminine hair growth.[link.springer.com]

  • Donohue Syndrome

    DS is characterized by pre- and postnatal growth retardation with failure to thrive, lipoatrophy, muscle wasting, acanthosis nigricans, hypertrichosis, and dysmorphic features[ncbi.nlm.nih.gov] ジュベー症候群 MarieJoubert Canadian neurologist Kahn カーン Kahn test カーンテスト Kallmann カルマン Kallmann syndrome カルマン症候群 Kaposi カポジ Kaposi's sarcoma カポジ肉腫 Móric Kaposi (1837 -1902) Hungarian[jams.med.or.jp] […] a rare and lethal autosomal recessive disease caused by mutations in the insulin receptor (INSR) gene, manifesting marked insulin resistance, severe growth retardation, hypertrichosis[ncbi.nlm.nih.gov]

  • Bagatelle-Cassidy Syndrome

    nigricans - Not a rare disease Acanthosis nigricans muscle cramps acral enlargement Acardia Acatalasemia Accessory deep peroneal nerve Accessory navicular bone - Not a rare[rarediseases.info.nih.gov] Juvenile primary lateral sclerosis Juvenile retinoschisis Juvenile-onset dystonia Kabuki syndrome Kallmann syndrome Kallmann syndrome 1 Kallmann syndrome 2 Kanzaki disease[rarediseases.info.nih.gov] […] syndrome Acrogeria, Gottron type Acrokeratoelastoidosis of Costa Acromegaloid facial appearance syndrome Acromegaloid features, overgrowth, cleft palate and hernia Acromegaloid hypertrichosis[rarediseases.info.nih.gov]

  • Michels-Caskey Syndrome

    nigricans - Not a rare disease Acanthosis nigricans muscle cramps acral enlargement Acardia Acatalasemia Accessory deep peroneal nerve Accessory navicular bone - Not a rare[rarediseases.info.nih.gov] Juvenile primary lateral sclerosis Juvenile retinoschisis Juvenile-onset dystonia Kabuki syndrome Kallmann syndrome Kallmann syndrome 1 Kallmann syndrome 2 Kanzaki disease[rarediseases.info.nih.gov] […] syndrome Acrogeria, Gottron type Acrokeratoelastoidosis of Costa Acromegaloid facial appearance syndrome Acromegaloid features, overgrowth, cleft palate and hernia Acromegaloid hypertrichosis[rarediseases.info.nih.gov]

  • Tollner-Horst-Manzke Syndrome

    nigricans - Not a rare disease Acanthosis nigricans muscle cramps acral enlargement Acardia Acatalasemia Accessory deep peroneal nerve Accessory navicular bone - Not a rare[rarediseases.info.nih.gov] Kaler Garrity Stern Syndrome Kallmann syndrome Kantaputra Gorlin Syndrome Kaplan Plauchu Fitch Syndrome Kaplowitz Bodurtha syndrome Kapur Toriello Syndrome Karak Syndrome[rgd.mcw.edu] […] syndrome Acrogeria, Gottron type Acrokeratoelastoidosis of Costa Acromegaloid facial appearance syndrome Acromegaloid features, overgrowth, cleft palate and hernia Acromegaloid hypertrichosis[rarediseases.info.nih.gov]

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