These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Association between Michelin tire baby syndrome and congenital panhyopituitarism in an Iranian girl. Haghshenas Z; Tajziehchi L; Ghavami F Arch Iran Med; 2014 Aug; 17(8):585-6. PubMed ID: 25065283 [TBL] [Abstract][Full Text] [Related]
6. Michelin tyre baby: a rare genodermatosis. Dhingra D; Sethi GR; Mantan M Indian Pediatr; 2013 Aug; 50(8):808. PubMed ID: 24036654 [No Abstract] [Full Text] [Related]
7. Michelin tire baby syndrome--a case report and literature review. Farooqi GA; Mulla SA; Ahmad M J Pak Med Assoc; 2010 Sep; 60(9):777-9. PubMed ID: 21381593 [TBL] [Abstract][Full Text] [Related]
8. Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene. Dentici ML; Terracciano A; Bellacchio E; Capolino R; Novelli A; Digilio MC; Dallapiccola B Clin Genet; 2018 Jun; 93(6):1223-1228. PubMed ID: 29427453 [TBL] [Abstract][Full Text] [Related]
9. Generalized smooth muscle hamartoma with multiple congenital anomalies without the "Michelin tire baby" phenotype. Janicke EC; Nazareth MR; Rothman IL Pediatr Dermatol; 2014; 31(6):731-3. PubMed ID: 24383769 [TBL] [Abstract][Full Text] [Related]
10. Michelin tire baby syndrome: a review of the literature and a proposal for diagnostic criteria with adoption of the name circumferential skin folds syndrome. Rothman IL Pediatr Dermatol; 2014; 31(6):659-63. PubMed ID: 25424205 [TBL] [Abstract][Full Text] [Related]
11. A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2. Feng J; Lan X; Shen J; Song X; Tang X; Xu W; Ren X; Zhang H; Yu G; Wu S Mol Genet Genomic Med; 2020 Feb; 8(2):e1096. PubMed ID: 31903734 [TBL] [Abstract][Full Text] [Related]
12. Michelin tire baby syndrome: a case report. Uzair M; Butt G; Khurshid K Int J Dermatol; 2015 Nov; 54(11):e476-7. PubMed ID: 26227104 [No Abstract] [Full Text] [Related]
17. Syndrome of congenital cutis laxa with ligamentous laxity and delayed development: report of a brother and sister from Turkey. Oğur G; Yüksel-Apak M; Demiryont M Am J Med Genet; 1990 Sep; 37(1):6-9. PubMed ID: 1700609 [TBL] [Abstract][Full Text] [Related]
18. Cutis laxa of the autosomal recessive type in a consanguineous family. de Schepper S; Loeys B; de Paepe A; Lambert J; Naeyaert JM Eur J Dermatol; 2003; 13(6):529-33. PubMed ID: 14721770 [TBL] [Abstract][Full Text] [Related]