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118 Possible Causes for arnhold

  • Leydig Cell Hypoplasia due to LHB Deficiency

    I.J....Bloise W. 1987 25 Male pseudohermaphroditism resulting from Leydig cell hypoplasia. ( 3998941 ) Arnhold I.J....Toledo S.P. 1985 26 Leydig cell hypoplasia causing male[malacards.org] Reviews Arnhold et al. (2009) noted that the clinical manifestations of female patients with hypogonadotropic hypogonadism due to isolated LH deficiency (HH23; 228300) are[ncbi.nlm.nih.gov] Reviews {1:Arnhold et al. (2009)} noted that the clinical manifestations of female patients with hypogonadotropic hypogonadism due to isolated LH deficiency (HH23; {228300[diseaseinfosearch.org]

  • Familial Male-Limited Precocious Puberty

    Brito VN, Latronico AC, Arnhold IJ, Mendonca BB. Update on the etiology, diagnosis and therapeutic management of sexual precocity. Arq Bras Endocrinol Metabol . 2008; .[rarediseases.info.nih.gov] […] gonadotrophin-independent sexual precocity GIPP gonadotrophin-independent precocious puberty precocious pseudopuberty pubertas praecox testotoxicosis Brito VN, Latronico AC, Arnhold[ghr.nlm.nih.gov] Latronico AC, Abell AN, Arnhold IJ et al.[link.springer.com]

  • 46,XY Disorder of Sex Development

    Journal Best Pract Res Clin Endocrinol Metab 22:119-34 (2008) DOI: 10.1016/j.beem.2007.11.001 Reference PMID: 18811725 Authors Mendonca BB, Domenice S, Arnhold IJ, Costa EM[genome.jp] ., (2007) The New England Journal Of Medicine 356 (3):237-247 (PMID: 17229951) Arnhold et al., (2009) Horm.[genedx.com]

  • Genetic Combined Pituitary Hormone Deficiencies

    Cogan JD, Wu W, Phillips JA 3rd, Arnhold IJ, Agapito A, Fofanova OV, Osorio MG, Bircan I, Moreno A, Mendonca BB: The PROP1 2-base pair deletion is a common cause of combined[karger.com] ., Arnhold, IJ., Kalina, MA., Kot K., Krzisnik, C., Lemos, MC., Malikova, J., Navardauskaite, R., Obermannova, B., Pribilincova, Z., Sallai, A., Stipancic, G., Verkauskiene[evolvegene.com] Arnhold, A. Agapito, O.V. Fofanova The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency [4] P. Duquesnoy, A. Roy, F. Dastot, I.[elsevier.pt]

  • Leydig Cell Hypoplasia

    I.J....Bloise W. 1987 25 Male pseudohermaphroditism resulting from Leydig cell hypoplasia. ( 3998941 ) Arnhold I.J....Toledo S.P. 1985 26 Leydig cell hypoplasia causing male[malacards.org] Reviews {1:Arnhold et al. (2009)} noted that the clinical manifestations of female patients with hypogonadotropic hypogonadism due to isolated LH deficiency (HH23; {228300[diseaseinfosearch.org] Arnhold, X. Liu, B. B. Mendonca & D. L.[doi.org]

  • Kallmann Syndrome Type 2

    ., (2007) The New England Journal Of Medicine 356 (3):237-247 (PMID: 17229951) Arnhold et al., (2009) Horm.[genedx.com]

  • Central Precocious Puberty Type 2

    Silveira LG, Noel SD, Silveira-Neto AP, Abreu AP, Brito VN, Santos MG, Bianco SD, Kuohung W, Xu S, Gryngarten M, Escobar ME, Arnhold IJ, Mendonca BB, Kaiser UB, Latronico[ghr.nlm.nih.gov] Brito VN, Batista MC, Borges MF, Latronico AC, Kohek MB, Thirone AC, Jorge BH, Arnhold IJ, Mendonca BB. (1999 Oct) Diagnostic value of fluorometric assays in the evaluation[labtestsonline.it] J Clin Endocrinol Metab 77:118-124 3. de Brito VN, Latronico AC, Arnhold IJ, Lo LS, Domenice S, Albano MC, Fragoso MC, Mendonca BB 1999 Treatment of gonadotropin dependent[hopeforhh.org]

  • Disorder of Sex Development - Intellectual Disability Syndrome

    F., Arnhold, I. J. P., Silva, F. A. Q., Nicolau, W., … Wilson, J. D. (2003).[link.springer.com] ., Arnhold, I. J. P. Batista, M. C., Pereira de Almeida Toleda S., Drummond M. C. F., … Mattar, E. (1987).[link.springer.com] B., Bloise, W., Arnhold, I. J. P. Batista, M. C., Pereira de Almeida Toleda S., Drummond M. C. F., … Mattar, E. (1987).[link.springer.com]

  • Noonan Syndrome

    Accessed May 11, 2012. 20301680 Jorge AA, Malaquias AC, Arnhold IJ, Mendonça BB.[labcorp.com] Prado Arnhold , Bases Genéticas dos Distúrbios de Crescimento , Arquivos Brasileiros de Endocrinologia & Metabologia , 46 , 4 , (444) , (2002) . Paul J.[doi.org] Article PubMed Malaquias AC, Brasil AS, Pereira AC, Arnhold IJ, Mendonca BB, Bertola DR and Jorge AA.[doi.org]

  • Leri-Weill Dyschondrosteosis

    Jorge AA, Nishi MY, Funari MF, Souza SC, Arnhold IJ, et al. Short stature caused by SHOX gene haploinsufficiency: from diagnosis to treatment.[degruyter.com] Scalco RC, Melo SS, Pugliese-Pires PN, Funari MF, Nishi MY, Arnhold IJ, et al.[e-apem.org] Funari MF, Jorge AA, Souza SC, Billerbeck AE, Arnhold IJ, et al. Usefulness of MLPA in the detection of SHOX deletions. Eur J Med Genet 2010;53:234–8.[degruyter.com]

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