Hypogonadotropic hypogonadism in a female with the Johnson-McMillin syndrome

American Journal of Obstetrics and Gynecology

Volumn 191, Issue 5, 2004, Pages 1728-1729

  De Metsenaere, Fleur ^a   Mortier, Geert ^b   Dhont, Marc ^a,b  

^a Depts of Obstetrics and Gynecology   (Belgium)

^b GHENT UNIVERSITY HOSPITAL   (Belgium)

Author keywords

Hypogonadotropic hypogonadism; Johnson McMillin syndrome; Oocyte donation

Indexed keywords

ADULT; ALOPECIA; ANOSMIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CLINICAL FEATURE; CONDUCTION DEAFNESS; DENTAL CARIES; DISEASE ASSOCIATION; FEMALE; HUMAN; HYPOGONADOTROPIC HYPOGONADISM; JOHNSON MCMILLIN SYNDROME; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; ADULT; AMENORRHEA; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; HYPOGONADISM; NEUROCUTANEOUS SYNDROMES;

EID: 8544224256     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajog.2004.06.040     Document Type: Article

References (3)

1. V.P. Johnson, J.M. McMillin, T. Aceto Jr., and G. Bruins A newly recognized neuroectodermal syndrome of familial alopecia, anosmia, deafness, and hypogonadism Am J Med Genet 15 1983 497 506
2. D.N. Schweitzer, S. Yano, D.L. Earl, and J.M. Graham Jr. Johnson-McMillin Syndrome, a neuroectodermal syndrome with conductive hearing loss and microtia: report of a new case Am J Med Genet 120A 2003 400 405
3. M.C. Johnston The neural crest in abnormalities of the face and brain D. Bergsma Morphogenesis and malformation of the face and brain 1975 Alan Liss for the National Foundation-March of Dimes New York 1 18 BD:OAS XI(7)