Results 81 to 90 of about 2,952 (186)

A Female Case of Kallmann's Syndrome

Endocrinologia Japonica, 1976
A case of 20-year-old woman with hypogonadotropic hypogonadism and anosmia is reported, since very few female cases of Kallmann's syndrome have been reported so far in Japan. Three uncles on the father's side had no children. Height was 168 cm, and arm span 165 cm. The olfactory test revealed complete anosmia. Bone age was 13 year. Chromosome was 46 XX
Etsuji Sowa, Masahisa Wada, Kazuko Iba, Bumpei Tanaka, Susumu Shiode, Hirotoshi Morii, Noboru Hamada, Kazutaka Hamada   +7 more
openaire   +4 more sources

A RARE ENDOCRINE CASE REPORT OF KALLMANN SYNDROME

Journal of University Medical & Dental College, 2017
: Kallmann syndrome is a rare disorder of secondary hypogonadism with or without anosmia/ hyposmia due to abnormal migration of gonadotrophin releasing hormone producing neurons in hypothalamus.
Nasir Mahmood
doaj  

A case of Kallmann syndrome associated with a non-functional pituitary microadenoma

Endocrinology, Diabetes & Metabolism Case Reports, 2018
Kallmann syndrome (KS) is a form of hypogonadotropic hypogonadism in combination with a defect in sense of smell, due to abnormal migration of gonadotropin-releasing hormone-producing neurons. We report a case of a 17-year-old Tunisian male who presented
Taieb Ach, Hela Marmouch, Dorra Elguiche, Asma Achour, Hajer Marzouk, Hanene Sayadi, Ines Khochtali, Mondher Golli   +7 more
doaj   +1 more source

A novel mutation of the KAL1 gene in monozygotic twins with Kallmann syndrome [PDF]

, 2000
Takeshi Matsuo, S Okamoto, Yukiko Izumi, A Hosokawa, Takashi TAKEGAWA, Hiroshi Fukui, Zaw Myo Tun, Kazuhiro Honda, Ryo Matoba, Koichi Tatsumi, Nobuyuki Amino   +10 more
openalex   +1 more source

Kallmann syndrome [PDF]

BMJ, 2012
Neil Smith, Richard Quinton
openaire   +3 more sources

Similar interstitial deletions of the KAL-1 gene in two Brazilian families with X-linked Kallmann Syndrome

Genetics and Molecular Biology, 2004
Mutations in the KAL-1 gene localized at Xp22.3 have been shown to be responsible for the X-linked Kallmann syndrome (KS), a disorder characterized by the association of hypogonadotropic hypogonadism and anosmia.
Ericka Barbosa Trarbach, Isabella Lopes Monlleo, Carlos Guilherme Gaelzer Porciuncula, Marshall Italo Barros Fontes, Maria Teresa Mathias Baptista, Christine Hackel   +5 more
doaj   +1 more source

The Importance of Autosomal Genes in Kallmann Syndrome: Genotype-Phenotype Correlations and Neuroendocrine Characteristics¹ [PDF]

, 2001
Luciana Mattos Barros Oliveira, Stephanie B. Seminara, Milena Beranova, Frances J. Hayes, Sarah B. Valkenburgh, Ernestina Schipani, Elaine Maria Frade Costa, Ana Cláudia Latronico, William F. Crowley, Mario Vallejo   +9 more
openalex   +1 more source

Psychological Aspects of Congenital Hypogonadotropic Hypogonadism

Frontiers in Endocrinology, 2019
Congenital hypogonadotropic hypogonadism/Kallmann syndrome (CHH/KS) is a rare, treatable form of infertility. Like other rare disease patients, individuals with CHH/KS frequently experience feelings of isolation, shame, and alienation.
Andrew A. Dwyer, Andrew A. Dwyer, Neil Smith, Richard Quinton   +3 more
doaj   +1 more source

The Importance of Autosomal Genes in Kallmann Syndrome: Genotype-Phenotype Correlations and Neuroendocrine Characteristics [PDF]

, 2001
Luciana Mattos Barros Oliveira
openalex   +1 more source

Nasal Placode Development, GnRH Neuronal Migration and Kallmann Syndrome

Frontiers in Cell and Developmental Biology, 2019
The development of Gonadotropin releasing hormone-1 (GnRH) neurons is important for a functional reproduction system in vertebrates. Disruption of GnRH results in hypogonadism and if accompanied by anosmia is termed Kallmann Syndrome (KS).
Hyun-Ju Cho, Yufei Shan, Niteace C. Whittington, Susan Wray   +3 more
doaj   +1 more source