Congenital Total Hemihypertrophy

Hemihypertrophy Spectrum

“…Barsky [24] and others found no report of familial occurrence. On the other hand, there have been many reports of familial hemihyperplasia in the literature with two or more affected relatives [24][25][26][27][28][29][30][31][32]. However, some of these patients had additional features, suggesting that not all of the families had IH [27].…”

Hemihypertrophy Spectrum

“…Barsky [24] and others found no report of familial occurrence. On the other hand, there have been many reports of familial hemihyperplasia in the literature with two or more affected relatives [24][25][26][27][28][29][30][31][32]. However, some of these patients had additional features, suggesting that not all of the families had IH [27].…”

A case of familial isolated hemihyperplasia

“…In this family, their maternal grandmother apparently had left facial hemihyperplasia but did not have mental retardation therefore it is unclear if the retardation was an unrelated finding. One other reported family showed a brother and sister with complete right-sided hemihyperplasia [8]. The brother had a history of seizures and the sister had mental retardation, nevi and strabismus.…”

Non‐syndromic hemihyperplasia in a male and his mother

“…Familial recurrence of non‐syndromic HHP is rare (Table II) [Reed, 1925; Scott, 1935; Arnold, 1936; Rudolph and Norvold, 1944; Morris and MacGillivray, 1955; Fraumeni et al, 1967; Meadows et al, 1974; Stoll et al, 1993] and in some case reports, affected status of other relatives has been anecdotal. We have summarized the features of reported familial cases in Table II.…”

Hemihypertrophy Spectrum

“…Barsky [24] and others found no report of familial occurrence. On the other hand, there have been many reports of familial hemihyperplasia in the literature with two or more affected relatives [24][25][26][27][28][29][30][31][32]. However, some of these patients had additional features, suggesting that not all of the families had IH [27].…”

A case of familial isolated hemihyperplasia

“…In this family, their maternal grandmother apparently had left facial hemihyperplasia but did not have mental retardation therefore it is unclear if the retardation was an unrelated finding. One other reported family showed a brother and sister with complete right-sided hemihyperplasia [8]. The brother had a history of seizures and the sister had mental retardation, nevi and strabismus.…”

Non‐syndromic hemihyperplasia in a male and his mother

“…Familial recurrence of non‐syndromic HHP is rare (Table II) [Reed, 1925; Scott, 1935; Arnold, 1936; Rudolph and Norvold, 1944; Morris and MacGillivray, 1955; Fraumeni et al, 1967; Meadows et al, 1974; Stoll et al, 1993] and in some case reports, affected status of other relatives has been anecdotal. We have summarized the features of reported familial cases in Table II.…”

Hemihypertrophy Spectrum

“…Barsky [24] and others found no report of familial occurrence. On the other hand, there have been many reports of familial hemihyperplasia in the literature with two or more affected relatives [24][25][26][27][28][29][30][31][32]. However, some of these patients had additional features, suggesting that not all of the families had IH [27].…”

A case of familial isolated hemihyperplasia

“…In this family, their maternal grandmother apparently had left facial hemihyperplasia but did not have mental retardation therefore it is unclear if the retardation was an unrelated finding. One other reported family showed a brother and sister with complete right-sided hemihyperplasia [8]. The brother had a history of seizures and the sister had mental retardation, nevi and strabismus.…”

Non‐syndromic hemihyperplasia in a male and his mother

“…Familial recurrence of non‐syndromic HHP is rare (Table II) [Reed, 1925; Scott, 1935; Arnold, 1936; Rudolph and Norvold, 1944; Morris and MacGillivray, 1955; Fraumeni et al, 1967; Meadows et al, 1974; Stoll et al, 1993] and in some case reports, affected status of other relatives has been anecdotal. We have summarized the features of reported familial cases in Table II.…”