Case report on a female patient with 17- -hydroxylase deficiency
Gassel, W.D.; Gerdes, H.; Littmann, K.P.
Verhandlungen der Deutschen Gesellschaft für Innere Medizin 77: 1057-1060
1971
ISSN/ISBN: 0070-4067 PMID: 4346174 Document Number: 34896
Document emailed within 1 workday
Related Documents
Vlaski, J.; Katanić, D.; Kavecan, I.; Dautović, S.; Vorgucin, I. 2008: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency--case report Medicinski Pregled 61(3-4): 183-186Mackenroth, T. 1986: Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood Der Internist 27(4): 274-278
Agboola-Abu, C.F.; Aligwekwe, P.K.; Olowu, A.O.; Kuku, S.F. 1999: Congenital adrenal hyperplasia due to 11-hydroxylase enzyme deficiency in three siblings. A brief report West African Journal of Medicine 18(2): 80-86
Simonin, G.; Palix, C.; Roulier, R.; Coignet, J. 1986: 21-hydroxylase deficiency: a case in a newborn revealing a maternal forme tardive Annales de Pediatrie 33(5): 423-427
Yabe, R.; Mizuno, K.; Ojima, M.; Ogawa, S.; Tani, M.; Niimura, S.; Watari, H.; Kunii, N.; Suenaga, K.; Yatabe, Y. 1987: A hitherto unreported case of 21-hydroxylase deficiency associated with Bartter's syndrome and a balanced 6-9 translocation Journal of Medicine 18(5-6): 333-349
Pierre-Jacques, H.; Glueck, C.J.; Mont, M.A.; Hungerford, D.S. 1997: Familial heterozygous protein-S deficiency in a patient who had multifocal osteonecrosis. A case report Journal of Bone and Joint Surgery. American Volume 79(7): 1079-1084
Babala, J.; Horn, F.; Plank, L.; Szépe, P.; Cingel, V.; Vidiscák, M.; Studený, S.; Siman, J. 2002: Maffucci's syndrome--case report of a 5-year-old female patient Rozhledy V Chirurgii: Mesicnik Ceskoslovenske Chirurgicke Spolecnosti 81(2): 88-92
Verani, D.A.; Badone, M.; Borella, T.; Garbaccio, G. 1990: A renal tumor in a female HIV-positive patient. A case report Minerva Medica 81(3 Suppl): 73-75
Ririe, D.G.; Cosgriff, T.M.; Martin, B. 1979: Central retinal vein occlusion in a patient with familial antithrombin III deficiency: case report Annals of Ophthalmology 11(12): 1841-1845
Inamura, T.; Nishio, S.; Matsukado, K.; Nagafuji, H.; Ikezaki, K.; Morioka, T.; Fukui, M. 1998: Epstein-Barr virus-associated malignant lymphoma in an immuno-deficiency patient: a case report No Shinkei Geka. Neurological Surgery 26(5): 443-447
De Marinis, L.; Mancini, A.; Saporosi, A.; Calabrò, F.; Massari, M.; Moneta, E.; Menini, E.; Barbarino, A. 1989: Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature Minerva Ginecologica 41(7): 337-342
Morović-Vergles, J.; Galesić, K.; Seferović, M.; Skobić, N. 2002: Still's disease in adulthood--case report of a female patient and review of the literature Reumatizam 49(1): 29-32
Zacharías, S.; Contreras, P. 1984: Hirsutism secondary to congenital adrenal hyperplasia caused by a 21-hydroxylase deficiency of late onset. a clinical case Revista Chilena de Obstetricia y Ginecologia 49(5): 295-299
Coughlin, G.P.; van Deth, A.G.; Ey, G.T.; Grant, A.K. 1977: Alpha1-antitrypsin deficiency--a literature review and a case report of a patient with chronic obstructive airways disease and cirrhosis Australian and New Zealand Journal of Medicine 7(4): 400-403
Hille, J.J.; Phillips, J.I.; Petit, J.C.; Simpson, R.H. 1985: Oral Kaposi's sarcoma in a patient with the acquired immune deficiency syndrome. A case report with notes on management and safety Journal of the Dental Association of South Africa 40(6): 321-325
Yi, D.Yong.; Kim, Y.Duck.; Chae, S.; Yun, S.Weon.; Choi, Y.Bae.; Lim, I.Seok. 2019: Copper deficiency-induced bicytopenia caused by poor compliance in a paediatric patient with chronic malnutrition: A case report Jpma. Journal of the Pakistan Medical Association 69(5): 722-724
Herrero-Velázquez, S.; Luis Guerrero-Peral, A.; Gámez-Leyva, G.; Fernández-Buey, M.Nieves.; Conde, A.; Rodríguez, M.; Rojo-Martínez, E.; Pascual, J.; Fernández-Herranz, M.Rosario.; Dalmau-Obrador, J. 2010: Encephalitis due to antibodies against the NMDA receptor. A case report of a female patient with no associated tumour and a literature review Revista de Neurologia 50(11): 661-666
Ogawa, K.; Shimizu, Y.; Tsuchihashi, K.; Kida, K.; Kanamaru, S.; Ito, N. 2018: Misdirection of an Indwelling Urethral Catheter into the Ureter in a Female Patient with Neurogenic Bladder : A Case Report Hinyokika Kiyo. Acta Urologica Japonica 64(3): 123-126
Shay, H.; Calhoon, S. 1995: A large splenic cyst in a middle-aged female patient: an unusual case report and review Journal of the Oklahoma State Medical Association 88(2): 59-61
Yamada, S.; Setsuda, O.; Shinoda, T.; Kuriyama, M.; Kanematsu, M.; Ban, Y.; Kawada, Y. 1991: Spontaneous rupture of the renal pelvis in a female patient with defect of the uterus and hypoplasia of the vagina: a case report Hinyokika Kiyo. Acta Urologica Japonica 37(3): 279-281