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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease

Fig. 2

Dysmorphic features and changing phenotype of patient 2. At the age of 14 months (a, b). Facial features including dolichocephaly, high prominent forehead, “senile-like” face, very thin sparse hair, full cheeks, thin upper and lower lip, low-set protruding ears, pointed chin, small teeth. (c) Newborn period, (d) 2-month-old, (e) 4-month-old, (f) 23-month-old

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