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Quoted phrase not found in phrase index: "Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome"
Page 1
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies.
Expert Rev Neurother. 2020 Jan;20(1):65-84. doi: 10.1080/14737175.2020.1699060. Epub 2019 Dec 12.
Expert Rev Neurother. 2020.
PMID: 31829048
Review.
New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affected population.Expert opinion: The improvements in molecular diagnostic tools allow us to identify the meticulous underlying etiology of leu …
New genetic methods and stem cell transplantation are also under investigation to further increase the quality and duration of life in affec …
Hypomyelination, hypogonadotropic hypogonadism, hypodontia - First Polish patient.
Bekiesinska-Figatowska M, Mierzewska H, Kuczynska-Zardzewialy A, Szczepanik E, Obersztyn E.
Bekiesinska-Figatowska M, et al.
Brain Dev. 2010 Aug;32(7):574-8. doi: 10.1016/j.braindev.2009.07.008. Epub 2009 Aug 22.
Brain Dev. 2010.
PMID: 19700253
The term 4H was suggested for the rare, novel entity with hypomyelination, hypogonadotropic hypogonadism and hypodontia. A combination of clinical findings with ataxia and endocrinological abnormalities, brain MRI and dentition history are crucial for the diagnosis. …
The term 4H was suggested for the rare, novel entity with hypomyelination, hypogonadotropic hypogonadism and hypodontia. A com …
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An Indian boy with a novel leukodystrophy: 4H syndrome.
Jauhari P, Sahu JK, Singhi P, Dayal D, Khandelwal N.
Jauhari P, et al.
J Child Neurol. 2014 Jan;29(1):135-8. doi: 10.1177/0883073812470737. Epub 2013 Jan 9.
J Child Neurol. 2014.
PMID: 23307887
4H syndrome is a rare and distinct leukodystrophy characterized by hypomyelination, hypogonadotropic hypogonadism, and hypodontia. Detecting signs of pubertal growth failure and abnormal dentition offer the clues to the diagnosis. We present an Indian boy wit …
4H syndrome is a rare and distinct leukodystrophy characterized by hypomyelination, hypogonadotropic hypogonadism, and …
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