Devriendt K - Search Results

1

Scalp skin lesion in Turner syndrome: more than lymphoedema?

Debeer A, Steenkiste E, Devriendt K, Morren M. Debeer A, et al. Among authors: devriendt k. Clin Dysmorphol. 2005 Jul;14(3):149-150. Clin Dysmorphol. 2005. PMID: 15930906

2

Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocation.

Lukusa T, Devriendt K, Jaeken J, Fryns JP. Lukusa T, et al. Among authors: devriendt k. Clin Dysmorphol. 1999 Jan;8(1):47-51. Clin Dysmorphol. 1999. PMID: 10327251

3

Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism.

Devriendt K, Keymolen K, Roelen L, Van Goethem G, Meireleire J, Fryns JP. Devriendt K, et al. Clin Dysmorphol. 2000 Apr;9(2):111-4. doi: 10.1097/00019605-200009020-00007. Clin Dysmorphol. 2000. PMID: 10826622

4

Congenital nasal piriform aperture stenosis as a rare manifestation of monosomy 1p36.

Breckpot J, Hermans R, Poorten VV, Vermeesch JR, Devriendt K. Breckpot J, et al. Among authors: devriendt k. Clin Dysmorphol. 2010 Apr;19(2):95-97. doi: 10.1097/MCD.0b013e328337589b. Clin Dysmorphol. 2010. PMID: 20186048 No abstract available.

5

Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report.

De Somer L, Wouters C, Morren MA, De Vos R, Van Den Oord J, Devriendt K, Meyts I. De Somer L, et al. Among authors: devriendt k. Orphanet J Rare Dis. 2010 Dec 8;5:37. doi: 10.1186/1750-1172-5-37. Orphanet J Rare Dis. 2010. PMID: 21143835 Free PMC article.

6

Sacrococcygeal appendage with femur: exoparasitic pyropagus twin, mature teratoma, or disorganization-like syndrome?

Mbuyi-Musanzayi S, Kasole TL, Muenze PK, Tshilobo PL, Kitenge TK, Ngombe LK, Katombe FT, Devriendt K. Mbuyi-Musanzayi S, et al. Among authors: devriendt k. Clin Dysmorphol. 2015 Oct;24(4):173-5. doi: 10.1097/MCD.0000000000000086. Clin Dysmorphol. 2015. PMID: 25945455 No abstract available.

7

Microtia in Cornelia de Lange syndrome: a case from Democratic Republic of the Congo.

Kayembe Kitenge T, Kasole Lubala T, Mbuyi-Musanzayi S, Kabamba Ngombe L, Katshiez Nawej C, Musa Obadia P, Banza Lubaba Nkulu C, Nemery B, Devriendt K. Kayembe Kitenge T, et al. Among authors: devriendt k. Clin Dysmorphol. 2016 Oct;25(4):178-80. doi: 10.1097/MCD.0000000000000129. Clin Dysmorphol. 2016. PMID: 27088280 No abstract available.

8

What should we tell parents? Congenital diaphragmatic hernia.

Russo FM, Debeer A, De Coppi P, Devriendt K, Crombag N, Hubble T, Power B, Benachi A, Deprest J. Russo FM, et al. Among authors: devriendt k. Prenat Diagn. 2022 Mar;42(3):398-407. doi: 10.1002/pd.5880. Epub 2021 Feb 18. Prenat Diagn. 2022. PMID: 33599313 Review.

9

Occipital Horn syndrome in a 2-year-old boy.

De Paepe A, Loeys B, Devriendt K, Fryns JP. De Paepe A, et al. Among authors: devriendt k. Clin Dysmorphol. 1999 Jul;8(3):179-83. Clin Dysmorphol. 1999. PMID: 10457850

10

Isolated terminal limb reduction defects: extending the clinical spectrum of Adams-Oliver syndrome and ARHGAP31 mutations.

Isrie M, Wuyts W, Van Esch H, Devriendt K. Isrie M, et al. Among authors: devriendt k. Am J Med Genet A. 2014 Jun;164A(6):1576-9. doi: 10.1002/ajmg.a.36486. Epub 2014 Mar 25. Am J Med Genet A. 2014. PMID: 24668619

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