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Child With Unusual Appearance, Inguinal Hernia, Accelerated Growth, and Developmental Delay

Child With Unusual Appearance, Inguinal Hernia, Accelerated Growth, and Developmental Delay

Figure 1 – This 10-month-old boy was evaluated for developmental delay, an enlarged abdomen, and splenomegaly.

A 10-month old white child was admitted for evaluation of an enlarged abdomen, splenomegaly, and developmental delay.

The child had a normal gestation and birth weight. He had a right hydrocele at birth and rapid scrotal enlargement at age 3 months that led to repair of a right inguinal hernia.

Physical examination revealed a large, somewhat lethargic child with unusual facies (Figure 1). Height, 32 inches (greater than the 97th percentile for age, 50th percentile for 18 months); weight, 24.5 lb (greater than the 97th percentile for age; 50th percentile for 16 months); and head circumference, 18.5 inches (50th percentile for 12 months). He had a small anterior fontanelle with prominent forehead, mild hypertelorism, a shallow nasal bridge with clear nasal mucus discharge, and a short neck.

The child’s hands had a spadelike configuration, with ulnar deviation of the wrists.

Neuromuscular examination revealed normal muscle strength, tone, and deep tendon reflexes. Cranial nerve function was intact.

The liver edge was palpable 3 to 4 cm below the right costal margin.

Genital examination revealed a left scrotal mass with bilaterally descended testes and a small external urethral meatus.

Figure 2 – The pedigree shows the affected boy (arrow) and several affected maternal uncles (filled squares).

Scattered maculopapular lesions were present over the patient’s scalp, face, and neck. There was no lymphadenopathy.

The hematocrit was 38%; hemoglobin, 12.6 g/dL. The white blood cell count was normal, with granulation of the leukocytes on peripheral smear. Bone marrow analysis showed metachromatic granulation of histiocytes and leukocyte precursors. Levels of cholesterol, calcium, phosphorus, and total bilirubin were normal, as were results of tests of liver functions, routine karyotyping, electrocardiography, and skeletal survey radiography.

A family history revealed several maternal uncles with short stature; they had large heads, protruding abdomens, limited joint extension, hearing loss, poor vision, hernias, and cardiac abnormalities (Figure 2). A maternal great-uncle also had similar symptoms.

To what genetic disorder does this profile point?


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