Cargando…

Kallmann syndrome: MRI findings

Kallmann syndrome (KS) is a disease clinically characterized by the association of hypogonadotrophic hypogonadism and anosmia or hyposmia. It is a neuronal migration disorder. Magnetic resonance (MR) imaging is used to visualize the olfactory tracts and to evaluate the olfactory sulci. Five patients...

Descripción completa

Detalles Bibliográficos
Autores principales:	Zaghouani, Houneida, Slim, Ines, Zina, Neila Ben, Mallat, Najoua, Tajouri, Houda, Kraiem, Chakib
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2013
Materias:	Brief Communication
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830283/ https://www.ncbi.nlm.nih.gov/pubmed/24251137 http://dx.doi.org/10.4103/2230-8210.119536

Ejemplares similares

Caseous calcification of the mitral annulus on MDCT: a rare intracardiac mass
por: Mallat, Najoua, et al.
Publicado: (2013)

Une cause rare de cervicalgie febrile
por: Alaya, Zeineb, et al.
Publicado: (2016)

Une localisation exceptionnelle de la tuberculose vertébrale Mal de Pott sous-occipital
por: Yahyaoui, Sana, et al.
Publicado: (2013)

Pneumomédiastin au cours d'une dermatomyosite, une entité rare: à propos d'un cas
por: Majdoub, Senda, et al.
Publicado: (2016)

Spontaneous intraperitoneal rupture of hepatic hydatid cyst: a rare cause of ascites
por: Limeme, Manel, et al.
Publicado: (2014)

A rare inborn error of metabolism associated with a Dandy–Walker malformation
por: Manel, Limeme, et al.
Publicado: (2012)

A novel missense variant of FGFR1 in a Japanese girl with Kallmann syndrome and holoprosencephaly
por: Uchida, Noboru, et al.
Publicado: (2022)

Ataxia and focal dystonia in Kallmann syndrome
por: Hernando‐Quintana, Natalia, et al.
Publicado: (2015)

Metabolomic alterations associated with Kallmann syndrome
por: Guo, Ye, et al.
Publicado: (2020)

Clinical and inheritance profiles of Kallmann syndrome in Jordan
por: AbuJbara, Mousa A, et al.
Publicado: (2004)

Kallmann Syndrome: Eugenics and the Man behind the Eponym
por: Benbassat, Carlos A.
Publicado: (2016)

Reversible Kallmann Syndrome: Rare Yet Real
por: Soumya, Sudarsanababu Lalitha, et al.
Publicado: (2019)

Recent advances in understanding and managing Kallmann syndrome
por: Swee, Du Soon, et al.
Publicado: (2021)

PROK2/PROKR2 Signaling and Kallmann Syndrome
por: Dodé, Catherine, et al.
Publicado: (2013)

Sublingual thyroid ectopy: similarities and differences with Kallmann syndrome
por: Van Vliet*, Guy, et al.
Publicado: (2015)

Testosterone-induced acne fulminans in twins with Kallmann's syndrome
por: Saint-Jean, Mélanie, et al.
Publicado: (2014)

Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption
por: Liu, Yujun, et al.
Publicado: (2021)

A case of Kallmann syndrome associated with a non-functional pituitary microadenoma
por: Ach, Taieb, et al.
Publicado: (2018)

Vertebral metastases from intracranial meningioma
por: Zaghouani, H, et al.
Publicado: (2014)

Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland
por: Laitinen, Eeva-Maria, et al.
Publicado: (2011)

Congenital Hypogonadotropic Hypogonadism and Kallmann Syndrome: Past, Present, and Future
por: Kim, Soo-Hyun
Publicado: (2015)

Seminal Plasma Lipidomics Profiling to Identify Signatures of Kallmann Syndrome
por: Li, Xiaogang, et al.
Publicado: (2021)

SOX10 Mutation Screening for 117 Patients with Kallmann Syndrome
por: Shima, Hirohito, et al.
Publicado: (2021)

X-linked recessive Kallmann syndrome: A case report
por: Zhang, Ping, et al.
Publicado: (2022)

A rare disease of Kallmann syndrome: A case report
por: Hilman, Syawaluddin, et al.
Publicado: (2023)

Primary Hepatic Lymphoma in a Patient with Chronic Hepatitis B
por: Mrabet, Soumaya, et al.
Publicado: (2020)

Neurological manifestations following cured malaria: don't forget post-malaria neurological syndrome
por: Bellazreg, Foued, et al.
Publicado: (2021)

Whole genome investigation of an atypical autism case identifies a novel ANOS1 mutation with subsequent diagnosis of Kallmann syndrome
por: Dawson, Paul A., et al.
Publicado: (2020)

Invertebrate Models of Kallmann Syndrome: Molecular Pathogenesis and New Disease Genes
por: Schiavi, Elia Di, et al.
Publicado: (2013)

The prevalence of intragenic deletions in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
por: Pedersen-White, Jennifer R., et al.
Publicado: (2008)

Functional dissection of the Drosophila Kallmann's syndrome protein DmKal-1
por: Andrenacci, Davide, et al.
Publicado: (2006)

Nasal Placode Development, GnRH Neuronal Migration and Kallmann Syndrome
por: Cho, Hyun-Ju, et al.
Publicado: (2019)

Kallmann syndrome with a Tyr113His PROKR2 mutation
por: Ha, Jeong-Ha, et al.
Publicado: (2017)

Bone metastasis as the first sign of gastric cancer
por: Ameur, Wafa Ben, et al.
Publicado: (2017)

Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2
por: Dodé, Catherine, et al.
Publicado: (2006)

Novel Microdeletion in the X Chromosome Leads to Kallmann Syndrome, Ichthyosis, Obesity, and Strabismus
por: Ma, Wanlu, et al.
Publicado: (2020)

Molecular diagnosis of Kallmann syndrome with diabetes by whole exome sequencing and bioinformatic approaches
por: Sun, Shuang-Shuang, et al.
Publicado: (2021)

A rare case of congenital fibrosis of extra ocular muscles with Kallmann syndrome
por: Yenugandula, Raman, et al.
Publicado: (2022)

THU201 Atypical Presentation Of Kallmann Syndrome With A Rare Genetic Mutation
por: Montgomery, Emily L, et al.
Publicado: (2023)

Resting-State fMRI findings in patients with first-Episode idiopathic epilepsy before and after treatment
por: Qiao, Peng-Fei, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_k97i9ivndjrmvjon3hd0i7r45j