Kallmann Syndrome 6
What's New
Last Posted: Nov 03, 2024
- Genetic Polymorphisms of Prokineticins and Prokineticin Receptors Associated with Human Disease.
Roberta Lattanzi, et al. Life (Basel, Switzerland) 2024 0 (10) - Genetic architecture of congenital hypogonadotropic hypogonadism: insights from analysis of a Portuguese cohort.
Josianne Nunes Carriço, et al. Human reproduction open 2024 0 (3) hoae053 - A novel mutation in ANOS1 in a Chinese family with Kallmann syndrome: Case report.
Rong Jiang, et al. Clinical case reports 2024 0 (5) e8860 - Clinical phenotype of a Kallmann syndrome patient with IL17RD and CPEB4 variants.
Jianmei Zhang, et al. Frontiers in endocrinology 2024 0 1343977 - CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct.
Isabelle Roux, et al. Human genetics 2023 0 - Genetic Analysis of Patients with Congenital Hypogonadotropic Hypogonadism: A Case Series.
Rossella Cannarella, et al. International journal of molecular sciences 2023 0 (8) - DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.
Bouilly Justine, et al. Human molecular genetics 2017 0 (2) 359-372 - Next-generation sequencing of patients with congenital anosmia.
Alkelai Anna, et al. European journal of human genetics : EJHG 2017 0 (12) 1377-1387 - Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations.
Nie Min, et al. European journal of endocrinology 2017 0 (4) 389-398 - Reconsidering olfactory bulb magnetic resonance patterns in Kallmann syndrome.
Hacquart Thomas, et al. Annales d'endocrinologie 2017 0 (5) 455-461
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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