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117 results

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Page 1
Pyoderma Gangrenosum: A Challenging Cutaneous Manifestation in Dubowitz Syndrome.
Ghode DB, Hirani S, Kenjale S, Heda A, Hirani S, Prasad R, Wanjari M. Ghode DB, et al. Cureus. 2023 Aug 13;15(8):e43408. doi: 10.7759/cureus.43408. eCollection 2023 Aug. Cureus. 2023. PMID: 37706150 Free PMC article. Review.
Pyoderma gangrenosum (PG) is a challenging cutaneous manifestation associated with Dubowitz syndrome, a rare genetic disorder characterized by multiple congenital anomalies, developmental delay, and distinctive facial features. ...Clinical characteristics of Pyoderm …
Pyoderma gangrenosum (PG) is a challenging cutaneous manifestation associated with Dubowitz syndrome, a rare genetic disorder …
The Dubowitz syndrome: further observations.
Orrison WW, Schnitzler ER, Chun RW. Orrison WW, et al. Am J Med Genet. 1980;7(2):155-70. doi: 10.1002/ajmg.1320070209. Am J Med Genet. 1980. PMID: 6258433 Review.
An autosomal recessive disorder characterized by intrauterine growth retardation, postnatal retardation, microcephaly, sparse hair, toe syndactyly, and characteristic facial appearance is now recognized as the Dubowitz syndrome. Five addition additional cases of the …
An autosomal recessive disorder characterized by intrauterine growth retardation, postnatal retardation, microcephaly, sparse hair, toe synd …
[Dubowitz syndrome].
Tsukahara M. Tsukahara M. Ryoikibetsu Shokogun Shirizu. 2001;(33):571-3. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11462575 Review. Japanese. No abstract available.
[Dubowitz syndrome].
Tsukahara M, Tsujino K. Tsukahara M, et al. Ryoikibetsu Shokogun Shirizu. 2000;(32):295-7. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212722 Review. Japanese. No abstract available.
[Dubowitz syndrome].
Hirano T. Hirano T. Ryoikibetsu Shokogun Shirizu. 2000;(30 Pt 5):173-4. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11057184 Review. Japanese. No abstract available.
[Dubowitz syndrome].
Belohradsky BH, Egger J, Meiswinkel M, Knoop M, Weiss M, Sauer O. Belohradsky BH, et al. Ergeb Inn Med Kinderheilkd. 1988;57:145-84. Ergeb Inn Med Kinderheilkd. 1988. PMID: 3063524 Review. German. No abstract available.
Dubowitz syndrome: possible evidence for a clinical subtype.
Ilyina HG, Lurie IW. Ilyina HG, et al. Am J Med Genet. 1990 Apr;35(4):561-5. doi: 10.1002/ajmg.1320350423. Am J Med Genet. 1990. PMID: 2185633 Review.
Clinico-genetic analysis of 21 personal observations and review of the literature confirmed the existence of a wide phenotypic spectrum of Dubowitz syndrome. It is shown that in spite of marked microcephaly, severe mental deficiency is rare in Dubowitz syn …
Clinico-genetic analysis of 21 personal observations and review of the literature confirmed the existence of a wide phenotypic spectrum of …
Dubowitz syndrome.
Winter RM. Winter RM. J Med Genet. 1986 Feb;23(1):11-3. doi: 10.1136/jmg.23.1.11. J Med Genet. 1986. PMID: 3950932 Free PMC article. No abstract available.
Dubowitz syndrome.
Wilhelm OL, Méhes K. Wilhelm OL, et al. Acta Paediatr Hung. 1986;27(1):67-75. Acta Paediatr Hung. 1986. PMID: 3730185
Four children including two siblings with Dubowitz syndrome are presented. All four were preterm or small-for-dates. On the basis of their symptoms, it is suggested that infantile eczema is not an essential sign of the disorder, whereas the high frequency of hernia, …
Four children including two siblings with Dubowitz syndrome are presented. All four were preterm or small-for-dates. On the ba …
117 results