Figure 2
From: Deletion mutation in BSCL2 gene underlies congenital generalized lipodystrophy in a Pakistani family
Clinical features of the patient (IV-1) with congenital generalized lipodystrophy. (a) Note curly scalp hair, hypodontia, abdominal distension, acanthosis nigricans, velvety thickening and hyperpigmentation of the skin around neck, in axillae and antecubital fossae (b) Hypertrophic muscles over calves and acanthosis nigricans in the popliteal fossae (c) Magnetic Resonance Imaging showing no exaggeration of the external or internal cerebrospinal fluid (CSF) spaces suggesting that brain atrophy is not evident.