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marfanoid body habitus相关文献:
Hypermobile Ehlers-Danlos Syndrome.
Hakim A.
2004 Oct 22 [updated 2024 Feb 22]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
PMID:20301456
Congenital Contractural Arachnodactyly.
Callewaert B.
2001 Jan 23 [updated 2022 Jul 14]. In: Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2026.
PMID:20301560
[A case of marfanoid body habitus associated with an excessive hyperextensibility of the skin--an unclassified case in inherited connective tissue diseases].
Sakatsume Y, Saito M, Hara Y, Maruno Y, Sato K, Ishii J, Saito N, Hashimoto H, Saito K, Shinkai H.
Nihon Naika Gakkai Zasshi. 1988 Apr;77(4):499-505. doi: 10.2169/naika.77.499.
PMID:3042899
How to Distinguish Marfan Syndrome from Marfanoid Habitus in a Physical Examination-Comparison of External Features in Patients with Marfan Syndrome and Marfanoid Habitus.
Wozniak-Mielczarek L, Osowicka M, Radtke-Lysek A, Drezek-Nojowicz M, Gilis-Malinowska N, Sabiniewicz A, Mielczarek M, Sabiniewicz R.
Int J Environ Res Public Health. 2022 Jan 11;19(2):772. doi: 10.3390/ijerph19020772.
PMID:35055593
Bilateral Anteriorly Displaced Microspherophakia in a Female Child With Marfanoid Habitus.
Khan TA, Khan AA, Khan A, Zahid MA, Mehboob MA.
Cureus. 2023 May 1;15(5):e38371. doi: 10.7759/cureus.38371. eCollection 2023 May.
PMID:37265880
Children with multiple endocrine neoplasia type 2B: Not tall and marfanoid, but short with normal body proportions.
van den Broek MFM, van Santen HM, Valk GD, Verrijn Stuart AA.
Clin Endocrinol (Oxf). 2021 Sep;95(3):453-459. doi: 10.1111/cen.14536. Epub 2021 Jul 12.
PMID:34160841
Lujan-Fryns Syndrome (LFS): A Unique Combination of Hypernasality, Marfanoid Body Habitus, and Neuropsychiatric Issues, Presenting as Acute-Onset Dysphagia.
Khan A, Humayun M, Haider I, Ayub M.
Clin Med Insights Case Rep. 2016 Dec 4;9:115-118. doi: 10.4137/CCRep.S41083. eCollection 2016.
PMID:27980443
Genetic counseling of families with Marfan syndrome and other disorders showing a Marfanoid body habitus.
Bard LA.
Ophthalmology. 1979 Oct;86(10):1764-93. doi: 10.1016/s0161-6420(79)35344-1.
PMID:317927
Pure mucosal neuroma syndrome, not MEN2B.
Subramaniam Y, de Benito-Llopis L, Sharma A.
BMJ Case Rep. 2025 Mar 24;18(3):e264458. doi: 10.1136/bcr-2024-264458.
PMID:40127961
3q27.3 microdeletional syndrome: a recognisable clinical entity associating dysmorphic features, marfanoid habitus, intellectual disability and psychosis with mood disorder.
Thevenon J, Callier P, Poquet H, Bache I, Menten B, Malan V, Cavaliere ML, Girod JP, Thauvin-Robinet C, El Chehadeh S, Pinoit JM, Huet F, Verges B, Petit JM, Mosca-Boidron AL, Marle N, Mugneret F, Masurel-Paulet A, Novelli A, Tümer Z, Loeys B, Lyonnet S, Faivre L.
J Med Genet. 2014 Jan;51(1):21-7. doi: 10.1136/jmedgenet-2013-101939. Epub 2013 Oct 16.
PMID:24133203
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