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Seckel syndrome with cutaneous pigmentary changes: two siblings and a review of the literature
Kılıç, Fatma Arzu; Çakmak, Seray Kulcu; Tuncalı, Timur; Koz, Özlem; Özhamamci, Esra; Yasun, Oztan; Artuz, Ferda (Termedia Publishing House Ltd, 2015)Seckel syndrome (SCKL) is an extremely rare form of primordial dwarfism characterized by growth delay, proportionate extreme short stature, a prominent beak-like nose, hypoplasia of the malar area, small chin, microcephaly, ...